Candy and gummies recalls: brands, lot codes and what to do
Short answer: FDA has listed 67 candy and gummies recalls reported since November 2024; the most recent was reported on Oct 28, 2026 (El Ruisenor De Mexico, Inc.). Recalls cover specific products, lots and dates. Compare your package with the list below.
Search all FDA food recalls by product, brand, UPC or lot code.
All 67 recalls
Recall details
El Ruisenor De Mexico, Inc. · Oct 28, 2026
- Product
- Jovy Gummy Worms Neon; packaged in 1lb plastic units. UPC 712199083411
- Why it was recalled
- undeclared allergen ingredient (Red#40, Yellow#5, Yellow#6, Blue#1)
- Recall class
- Class II. Class II means the product may cause temporary or medically reversible health problems, and the chance of serious harm is remote.
- Lot codes and dates
- lot: 6156
- How many
- 521 pounds
- Where it was sold
- Recalling firm distributes primarily to California customers both retail and wholesale. Additional distribution to limited customers in Hawaii, Illinois, Kansas, Nevada, Oregon, and Washington.
- Status
- Ongoing: the recall is still active.
- Dates
- Recall started Aug 24, 2026; FDA classified it on Oct 20, 2026; reported in FDA's enforcement report on Oct 28, 2026.
- FDA recall number
- H-0130-2027
El Ruisenor De Mexico, Inc. · Oct 28, 2026
- Product
- Jovy Gummy Bears Regular; packed in a clear plastic 1lb unit sizes. UPC: UPC 712199085156
- Why it was recalled
- undeclared allergen ingredient (Red#40, Yellow#5, Yellow#6, Blue#1)
- Recall class
- Class II. Class II means the product may cause temporary or medically reversible health problems, and the chance of serious harm is remote.
- Lot codes and dates
- Lot: 6155
- How many
- 516 pounds
- Where it was sold
- Recalling firm distributes primarily to California customers both retail and wholesale. Additional distribution to limited customers in Hawaii, Illinois, Kansas, Nevada, Oregon, and Washington.
- Status
- Ongoing: the recall is still active.
- Dates
- Recall started Aug 24, 2026; FDA classified it on Oct 20, 2026; reported in FDA's enforcement report on Oct 28, 2026.
- FDA recall number
- H-0129-2027
El Ruisenor De Mexico, Inc. · Oct 28, 2026
- Product
- Jovy Gummy Peach Rings; packed in a clear plastic 1lb unit sizes. UPC: 712199083404
- Why it was recalled
- undeclared allergen ingredient (Red#40, Yellow#5, Yellow#6)
- Recall class
- Class II. Class II means the product may cause temporary or medically reversible health problems, and the chance of serious harm is remote.
- Lot codes and dates
- lot: 6124
- How many
- 687 pounds
- Where it was sold
- Recalling firm distributes primarily to California customers both retail and wholesale. Additional distribution to limited customers in Hawaii, Illinois, Kansas, Nevada, Oregon, and Washington.
- Status
- Ongoing: the recall is still active.
- Dates
- Recall started Aug 24, 2026; FDA classified it on Oct 20, 2026; reported in FDA's enforcement report on Oct 28, 2026.
- FDA recall number
- H-0125-2027
El Ruisenor De Mexico, Inc. · Oct 28, 2026
- Product
- Jovy Gummy Bears Neon; packed in 1lb plastic units. UPC 712199083558
- Why it was recalled
- undeclared allergen ingredient (Red#40, Yellow#5, Yellow#6, Blue#1)
- Recall class
- Class II. Class II means the product may cause temporary or medically reversible health problems, and the chance of serious harm is remote.
- Lot codes and dates
- Lot: 5120
- How many
- 127 pounds
- Where it was sold
- Recalling firm distributes primarily to California customers both retail and wholesale. Additional distribution to limited customers in Hawaii, Illinois, Kansas, Nevada, Oregon, and Washington.
- Status
- Ongoing: the recall is still active.
- Dates
- Recall started Aug 24, 2026; FDA classified it on Oct 20, 2026; reported in FDA's enforcement report on Oct 28, 2026.
- FDA recall number
- H-0128-2027
El Ruisenor De Mexico, Inc. · Oct 28, 2026
- Product
- Jovy Gummy Worms (Regular); packaged in 1lb plastic units. UPC: 712199083398
- Why it was recalled
- undeclared allergen ingredient (Red#40, Yellow#5, Yellow#6, Blue#1)
- Recall class
- Class II. Class II means the product may cause temporary or medically reversible health problems, and the chance of serious harm is remote.
- Lot codes and dates
- lot: 6087
- How many
- 327 pounds
- Where it was sold
- Recalling firm distributes primarily to California customers both retail and wholesale. Additional distribution to limited customers in Hawaii, Illinois, Kansas, Nevada, Oregon, and Washington.
- Status
- Ongoing: the recall is still active.
- Dates
- Recall started Aug 24, 2026; FDA classified it on Oct 20, 2026; reported in FDA's enforcement report on Oct 28, 2026.
- FDA recall number
- H-0131-2027
El Ruisenor De Mexico, Inc. · Oct 28, 2026
- Product
- Jovy Watermelon Gummy Rings; packed in a clear plastic 1lb unit sizes. UPC 712199083510
- Why it was recalled
- undeclared allergen ingredient (Red#40)
- Recall class
- Class III. Class III is FDA's lowest-risk category: the product is not likely to cause health problems.
- Lot codes and dates
- Lot: 6101
- How many
- 1,395 pounds
- Where it was sold
- Recalling firm distributes primarily to California customers both retail and wholesale. Additional distribution to limited customers in Hawaii, Illinois, Kansas, Nevada, Oregon, and Washington.
- Status
- Ongoing: the recall is still active.
- Dates
- Recall started Aug 24, 2026; FDA classified it on Oct 20, 2026; reported in FDA's enforcement report on Oct 28, 2026.
- FDA recall number
- H-0127-2027
SLT Foods Inc. · Oct 7, 2026
- Product
- Khazana The Treasure Spice Magic Fennel Candy, 5 lbs., Poly Plastic Bag, 4 per case
- Why it was recalled
- Undeclared Yellow 5 & 6, Red 3, and Blue 1
- Recall class
- Class II. Class II means the product may cause temporary or medically reversible health problems, and the chance of serious harm is remote.
- Lot codes and dates
- SLT-11-015
- How many
- 1 case
- Where it was sold
- The product was distributed to: NY
- Status
- Ongoing: the recall is still active.
- Dates
- Recall started Jul 10, 2026; FDA classified it on Oct 1, 2026; reported in FDA's enforcement report on Oct 7, 2026.
- FDA recall number
- H-0001-2027
Tiffany Food Corp · Sep 23, 2026
- Product
- Hexing Haw Balls candy; packaged in 200g/0.44 lb./7.05 oz clear plastic bag; Ingredients: haw, white sugar, water.; Serving suggestion: ready to eat. Storage: keep in cool and dry place and keep tightly closed in refrigerator after opening.; PRODUCT OF CHINA; UPC 6 920603 810025
- Why it was recalled
- Unapproved dye Ponceau 4R
- Recall class
- Class III. Class III is FDA's lowest-risk category: the product is not likely to cause health problems.
- Lot codes and dates
- Best Before 10/01/2026
- How many
- 38 cartons
- Where it was sold
- AZ, NY, CA, FL, GA, IL, MA, MN, NC, NJ, OH, PA, NY, TN, TX, VA
- Status
- Ongoing: the recall is still active.
- Dates
- Recall started Aug 28, 2026; FDA classified it on Sep 17, 2026; reported in FDA's enforcement report on Sep 23, 2026.
- FDA recall number
- H-1387-2026
Western Mixers Produce & Nuts, Inc. · Jul 8, 2026
- Product
- FIRST STREET Dark Chocolate Raisins Net Wt. 9 oz. (255g) UPC 797565011830 INGREDIENTS: DARK CHOCOLATE (SUGAR, CHOCOLATE LIQUOR, COCOA BUTTER, MILK FAT, SOY LECITHIN - AN EMULSIFIER, NATURAL VANILLA FLAVOR), RAISINS, TAPIOCA DEXTRIN, CONFECTIONERS GLAZE. CONTAINS: MILK, SOY PACKED IN A FAICLITY THAT HANDLES PEANUTS, TREE NUTS, WHEAT, SOY, EGG, SESAME, AND MILK PRODUCTS.
- Why it was recalled
- Undeclared peanuts. People who are allergic to peanuts run the risk of a serious or life-threatening allergic reaction if they eat this product.
- Recall class
- Class I. Class I is FDA's most serious category: a reasonable chance that eating or using the product will cause serious health problems or death.
- Lot codes and dates
- Lot: 260562 BB: 022527
- How many
- 29 cases (6 - 9oz packages/case) = 174 packages
- Where it was sold
- Product was distributed to a single retail customer who further distributed product to their California located stores.
- Status
- Ongoing: the recall is still active.
- Dates
- Recall started Jun 15, 2026; FDA classified it on Jun 26, 2026; reported in FDA's enforcement report on Jul 8, 2026.
- FDA recall number
- H-1125-2026
Dkiru LLC · Jun 24, 2026
- Product
- Adndale Magnesium Glycinate Gummies 400 mg. Plastic bottle containing 90 gummies. Net weight: 11.36 ounces. Serving size: 2 gummies. UPC: 860008784551 Firm name and address listed on label: Dkiru Ltd, Keepers Cottage, 3 Dublin Rd, Leixlip, Co. Kildare W23 H3C4, Ireland
- Why it was recalled
- Undeclared melatonin.
- Recall class
- Class II. Class II means the product may cause temporary or medically reversible health problems, and the chance of serious harm is remote.
- Lot codes and dates
- LOT 190824 Expiration Date: 08/19/2026, LOT 240923 Expiration Date: 09/22/2026, and LOT 240929 Expiration Date: 09/28/2026
- How many
- 13,920 bottles
- Where it was sold
- Will be provided when available.
- Status
- Ongoing: the recall is still active.
- Dates
- Recall started May 12, 2026; FDA classified it on Jun 18, 2026; reported in FDA's enforcement report on Jun 24, 2026.
- FDA recall number
- H-1079-2026
Raja Foods and Vegetables Inc. · May 20, 2026
- Product
- Swad Mango Flavored Masala Candy
- Why it was recalled
- Contains undeclared Blue 1
- Recall class
- Class II. Class II means the product may cause temporary or medically reversible health problems, and the chance of serious harm is remote.
- Lot codes and dates
- Lot: RF CA25301 UPC: 5117939557 Use by: APRIL 2027
- How many
- 205 cases (24 units per case)
- Where it was sold
- NY, NJ, DE, MA, PA, MD, CT, CA, NH, VT,
- Status
- Terminated: FDA has closed the recall.
- Dates
- Recall started Apr 13, 2026; FDA classified it on May 13, 2026; reported in FDA's enforcement report on May 20, 2026.
- FDA recall number
- H-0778-2026
Raja Foods and Vegetables Inc. · May 20, 2026
- Product
- Swad Orange Flavored Masala Candy
- Why it was recalled
- Contains undeclared FD&C Yellow 6
- Recall class
- Class II. Class II means the product may cause temporary or medically reversible health problems, and the chance of serious harm is remote.
- Lot codes and dates
- Lot: RF CA25233 UPC Codes: 5117939577 Use by: FEBRUARY 2027
- How many
- 205 CASES (24 units per case)
- Where it was sold
- NY, NJ, DE, MA, PA, MD, CT, CA, NH, VT,
- Status
- Terminated: FDA has closed the recall.
- Dates
- Recall started Apr 13, 2026; FDA classified it on May 13, 2026; reported in FDA's enforcement report on May 20, 2026.
- FDA recall number
- H-0777-2026
SB FOOD LLC · Mar 4, 2026
- Product
- Yoyo Gummy Grape Plus Flavor, 2.8 Oz (80g) , Plastic Bag, 24 bags per case
- Why it was recalled
- The products contain an unallowed color Carmoisine (E122) - Acid Red 14.
- Recall class
- Class II. Class II means the product may cause temporary or medically reversible health problems, and the chance of serious harm is remote.
- Lot codes and dates
- 11/11/24
- How many
- 100 Cases
- Where it was sold
- The adulterated product was distributed to the following states: AR, GA, IA, IN, KY, MD, MN, NE, NY, OH, PA, TN, TX, VA, WA.
- Status
- Ongoing: the recall is still active.
- Dates
- Recall started Nov 21, 2025; FDA classified it on Feb 25, 2026; reported in FDA's enforcement report on Mar 4, 2026.
- FDA recall number
- H-0529-2026
J2C Hawaii LLC · Mar 4, 2026
- Product
- Tiki Bar Candy Dark Chocolatey Peanut Butter & Pretzel. Net wt: Approx: 2 oz (57g). UPC 8 55725 00514 0. Taste of Maui Snacks dba of J2C Hawaii, LLC PO Box 1023, Wailuku HI 96793. The product label is read in parts: ***INGREDIENTS: Sugar***Whey Powder, Nonfat Milk Powder, Soy Lecithin***Peanut Butter (peanuts, peanut oil***), Pretzels (wheat flour***buttermilk solids***CONTAINS MILK AND SOY ***May contain wheat, peanuts and tree nuts***"
- Why it was recalled
- Ingredients List declares peanut but the Contains statement does not declare peanut
- Recall class
- Class II. Class II means the product may cause temporary or medically reversible health problems, and the chance of serious harm is remote.
- Lot codes and dates
- All packages with BB 11/26 or before
- How many
- 300 units
- Where it was sold
- Distributed in HI only.
- Status
- Terminated: FDA has closed the recall.
- Dates
- Recall started Jan 30, 2026; FDA classified it on Feb 24, 2026; reported in FDA's enforcement report on Mar 4, 2026.
- FDA recall number
- H-0523-2026
SB FOOD LLC · Mar 4, 2026
- Product
- Yoyo Gummy Tropical Flavor, 2.8 Oz (80g) , Plastic Bag, 24 bags per case
- Why it was recalled
- The products contain an unallowed color Carmoisine (E122) - Acid Red 14.
- Recall class
- Class II. Class II means the product may cause temporary or medically reversible health problems, and the chance of serious harm is remote.
- Lot codes and dates
- 11/11/24
- How many
- 100 Cases
- Where it was sold
- The adulterated product was distributed to the following states: AR, GA, IA, IN, KY, MD, MN, NE, NY, OH, PA, TN, TX, VA, WA.
- Status
- Ongoing: the recall is still active.
- Dates
- Recall started Nov 21, 2025; FDA classified it on Feb 25, 2026; reported in FDA's enforcement report on Mar 4, 2026.
- FDA recall number
- H-0528-2026
SB FOOD LLC · Mar 4, 2026
- Product
- Yoyo Gummy Assorted Flavor, 2.8 Oz (80g) , Plastic Bag, 24 bags per case
- Why it was recalled
- The products contain an unallowed color Carmoisine (E122) - Acid Red 14.
- Recall class
- Class II. Class II means the product may cause temporary or medically reversible health problems, and the chance of serious harm is remote.
- Lot codes and dates
- 11/11/24
- How many
- 100 Cases
- Where it was sold
- The adulterated product was distributed to the following states: AR, GA, IA, IN, KY, MD, MN, NE, NY, OH, PA, TN, TX, VA, WA.
- Status
- Ongoing: the recall is still active.
- Dates
- Recall started Nov 21, 2025; FDA classified it on Feb 25, 2026; reported in FDA's enforcement report on Mar 4, 2026.
- FDA recall number
- H-0527-2026
Beacon Promotions Inc · Feb 11, 2026
- Product
- Repackaged M&Ms candies, Net Wt 1.3 oz. Item BB458BG. Labeled with the following promotional company names. 1. Next Up, 2. Smith Pro, 3. Jaxport, Jacksonville Port Authority, 4. Climax Molybdenum, A Freeport-McMoRan Company, 5. University of Maryland, School of Public Policy, 6. Liberty University Environmental Health & Safety, 7. Subaru, 8. Trinity Cyb3r, 9. Candy Treats, 10. JSE, Jordan & Skala Engineers, 11. Dropbox DocSend, 12. PP, Prosperity Promotions, 13. Northwest Indian College Foundation, 14. FES Branding Solutions, 15. Berkshire Hathaway Guard Insurance Companies, 16. merry maids Annual 26 Conference, 17. BW, Best Western, 18. Morgan Stanley, 19. tufin, 20. Compliments of Pioneer, 21. A.D. Morgan, Construction Manager, Design Builder, General Contractor, 22. Adobe, 23. xfinity, 24. Fundermax Interiors, 25. White Cup, 26. Acadia Commercial, 27. Aviagen, 28. ORG Expo, 29. Make Your Mark For nutrition facts, information, and ingredients, go to https://hpgbrands.com/sugarspot-nutrition/
- Why it was recalled
- Undeclared allergens (milk, soy, and peanut) People who are allergic or sensitive to milk run the risk of a serious or life-threatening allergic reaction if they eat this product.
- Recall class
- Class II. Class II means the product may cause temporary or medically reversible health problems, and the chance of serious harm is remote.
- Lot codes and dates
- Lot L450ARCLV03, Best By 12/1/2025 Lot L502FLHKP01, Best By 1/1/2026 Lot L523CMHKP01, Best By 6/30/2026 Lot L537GMHKP01, Best By 9/1/2026
- How many
- 5788 units
- Where it was sold
- AL, AZ, CA, FL, IA, KS, KY, MA, MD, MN, NC, NY, OH, PA, SD, TN, TX, VA, WA, WI
- Status
- Ongoing: the recall is still active.
- Dates
- Recall started Jan 26, 2026; FDA classified it on Feb 4, 2026; reported in FDA's enforcement report on Feb 11, 2026.
- FDA recall number
- H-0462-2026
Beacon Promotions Inc · Feb 11, 2026
- Product
- Repackaged M&Ms Peanut candies, Net Wt 1.3 oz. Item BB471BG. Labeled as Make Your Mark. For nutrition facts information and ingredients, go to https://hpgbrands.com/sugarspot-nutrition/
- Why it was recalled
- Undeclared allergens (milk, soy, and peanut) People who are allergic or sensitive to milk run the risk of a serious or life-threatening allergic reaction if they eat this product.
- Recall class
- Class II. Class II means the product may cause temporary or medically reversible health problems, and the chance of serious harm is remote.
- Lot codes and dates
- Lot M1823200, Best By dates: 4/30/2026
- How many
- 541 units
- Where it was sold
- AL, AZ, CA, FL, IA, KS, KY, MA, MD, MN, NC, NY, OH, PA, SD, TN, TX, VA, WA, WI
- Status
- Ongoing: the recall is still active.
- Dates
- Recall started Jan 26, 2026; FDA classified it on Feb 4, 2026; reported in FDA's enforcement report on Feb 11, 2026.
- FDA recall number
- H-0461-2026
Fazt & Loud LLC · Feb 11, 2026
- Product
- Lost and Found Energy, Sour Gummy Bear, 12pck, 16oz Cans Case UPC: 850075595655 Can UPC: 850075595662 Aluminum Can Packaged
- Why it was recalled
- Recall is due to a misprint on the label that incorrectly identifies the total caffeine content on the can. The item contains 300mg of caffeine, instead of 150mg as provided on the can.
- Recall class
- Class III. Class III is FDA's lowest-risk category: the product is not likely to cause health problems.
- Lot codes and dates
- LOT #: MO-00911 BB Date: 11/13/2027
- How many
- N/A
- Where it was sold
- Nationwide
- Status
- Ongoing: the recall is still active.
- Dates
- Recall started Dec 2, 2025; FDA classified it on Feb 2, 2026; reported in FDA's enforcement report on Feb 11, 2026.
- FDA recall number
- H-0441-2026
GOLD STAR DISTRIBUTION INC · Jan 28, 2026
- Product
- All human food products distributed from the firm. Including but not limited to: snack foods, candy, gum, cooking oil, canned fruit and beans, honey, Dietary supplements, peanut butter, oatmeal, rice, dry peas and beans, ramen, cold cereal, hot sauce, lemon juice, crackers, canned sardines tuna and Oyster, sauces, seasonings, sugar, bottled and canned beverages, coffee and filters and creamer, tea bags, canned pasta, dates, flour, baby food
- Why it was recalled
- Potential exposure of rodents and rodent activity in the distribution center.
- Recall class
- Class II. Class II means the product may cause temporary or medically reversible health problems, and the chance of serious harm is remote.
- Lot codes and dates
- all codes of products purchased from this firm.
- How many
- unknown
- Where it was sold
- IN, MN, ND
- Status
- Ongoing: the recall is still active.
- Dates
- Recall started Dec 26, 2025; FDA classified it on Jan 22, 2026; reported in FDA's enforcement report on Jan 28, 2026.
- FDA recall number
- H-0411-2026
Tom Bumble LLC · Jan 7, 2026
- Product
- Tom Bumble Nutty Peanut Butter Flake Candy with Peanut & Chocolate GF V. Product is shelf stable, gold foil wrapping with paper label and cardboard outer box in some cases. Oregon Bark 2630 NE Sandy Blvd. Portland, Oregon 97232 2 Bars Boxes marked 50/50 or Nutty 4 Bars Boxes marked 50/50 or NUTTY 24 count boxes labeled Nutty UPC 852905007024 (1.2oz) UPC 852905007055 (2.2oz) UPC 852905007031 (4.5oz)
- Why it was recalled
- Foreign material. Pieces of foreign material in food can cause injuries such as cuts to the mouth or choking.
- Recall class
- Class II. Class II means the product may cause temporary or medically reversible health problems, and the chance of serious harm is remote.
- Lot codes and dates
- Best By dates between 5/21/26 - 6/9/26.
- How many
- Approx. 6500 units
- Where it was sold
- Distributed nationwide
- Status
- Terminated: FDA has closed the recall.
- Dates
- Recall started Dec 13, 2025; FDA classified it on Jan 12, 2026; reported in FDA's enforcement report on Jan 7, 2026.
- FDA recall number
- H-0391-2026
Bendon Publishing · Jan 7, 2026
- Product
- 1) Paw Patrol Heart-Shaped Gummy Candies, Mixed Fruit, Net Wt. 7 oz (200g), packaged in a cardboard box with heart-shaped top, UPC 805219643846, Distributed by Bendon, Inc. 2) Mickey Mouse Heart-Shaped Gummies, Mixed Fruit, Net Wt. 7 oz (200g), packaged in a cardboard box with heart-shaped top, UPC 805219643853, Distributed by Bendon, Inc. 3) Stitch Heart-Shaped Gummies, Tropical, Net Wt. 7 oz (200g), packaged in a cardboard box with heart-shaped top, UPC 805219643860, Distributed by Bendon, Inc. 4) SpongeBob Squarepants Heart-Shaped Gummy Candy, Tropical, Net Wt. 7 oz (200g), packaged in a cardboard box with heart-shaped top, UPC 805219644225, Distributed by Bendon, Inc. 5) Toy Story Multipack Size Gummies, Mixed Fruit, Net Wt. 6.35 oz (180g), packaged in a plastic bag containing 20 mini size packs (0.4 oz each), UPC 805219643914, Distributed by Bendon, Inc.
- Why it was recalled
- Unapproved color additive - chlorophyllin copper complex
- Recall class
- Class III. Class III is FDA's lowest-risk category: the product is not likely to cause health problems.
- Lot codes and dates
- 1) Lot# 3514-8A; Best Before 08/19/2027; Internal Item#: PC64384-WMPDQ 2) Lot# 3514-8B; Best Before 08/19/2027; Internal Item#: PC64385-WMPDQ 3) Lot# 3514-8C; Best Before 08/19/2027; Internal Item#: PC64386-WMPDQ 4) Lot# 3514-8D; Best Before 08/19/2027; Internal Item#: PC64422-WMPDQ 5) Lot# 3514-8E; Best Before 08/19/2027; Internal Item#: PC64391-WMPDQ
- How many
- 39,171 individual units (TOTAL)
- Where it was sold
- Distributors in FL, MN, TX, WA
- Status
- Terminated: FDA has closed the recall.
- Dates
- Recall started Dec 3, 2025; FDA classified it on Dec 29, 2025; reported in FDA's enforcement report on Jan 7, 2026.
- FDA recall number
- H-0350-2026
Zingerman's Coffee Company · Nov 19, 2025
- Product
- Zingerman's Peanut Butter Crush Candy Bar net wt 2oz UPC 844397005237
- Why it was recalled
- Undeclared cashew People who are allergic to tree nuts run the risk of a serious or life-threatening allergic reaction if they eat this product.
- Recall class
- Class I. Class I is FDA's most serious category: a reasonable chance that eating or using the product will cause serious health problems or death.
- Lot codes and dates
- Lot#174250
- How many
- 156 units
- Where it was sold
- This product was distributed to retailers in Michigan and New York and it reached consumers via retail stores.
- Status
- Terminated: FDA has closed the recall.
- Dates
- Recall started Sep 3, 2025; FDA classified it on Nov 10, 2025; reported in FDA's enforcement report on Nov 19, 2025.
- FDA recall number
- H-0178-2026
Zingerman's Coffee Company · Nov 19, 2025
- Product
- Zingerman's Ca$hew Cow Candy Bar net wt 2oz UPC 844397000157
- Why it was recalled
- Undeclared peanut People who are allergic to peanuts run the risk of a serious or life-threatening allergic reaction if they eat this product.
- Recall class
- Class I. Class I is FDA's most serious category: a reasonable chance that eating or using the product will cause serious health problems or death.
- Lot codes and dates
- Lot#174250
- How many
- 78 units
- Where it was sold
- This product was distributed to retailers in Michigan and New York and it reached consumers via retail stores.
- Status
- Terminated: FDA has closed the recall.
- Dates
- Recall started Sep 3, 2025; FDA classified it on Nov 10, 2025; reported in FDA's enforcement report on Nov 19, 2025.
- FDA recall number
- H-0179-2026
Abdallah Incorporated · Oct 29, 2025
- Product
- Lunds & Byerly's Premium confections. Pecan Caramel Cluster Dipped in milk chocolate. Net Wt 2.5 oz (71g) UPC 0 72431-01294 5. Produced for Lunds & Byerlys, Edina, MN 55424.
- Why it was recalled
- Pecan Caramel Clusters may contain undeclared cashews. People who are allergic to tree nuts run the risk of a serious or life-threatening allergic reaction if they eat this product.
- Recall class
- Class II. Class II means the product may cause temporary or medically reversible health problems, and the chance of serious harm is remote.
- Lot codes and dates
- Lot Number: 079Y Best By Date: Jan 29, 2026
- How many
- 744 units
- Where it was sold
- MN
- Status
- Terminated: FDA has closed the recall.
- Dates
- Recall started Sep 30, 2025; FDA classified it on Oct 20, 2025; reported in FDA's enforcement report on Oct 29, 2025.
- FDA recall number
- H-0099-2026
Vitalabs, Inc. · Oct 8, 2025
- Product
- vitamins B12 dietary supplement Raspberry Flavored sold under the following brand names: 1. Black Girl Vitamins 60 gummies UPC 8 60008 57505 0 Manufactured for: Black Girl Vitamins 601 W Harrison St., Chicago, IL 60607. 2. Rise-N-Shine 17 Woodport Road, Sparta, NJ 07871 UPC 8 99130 01189 1
- Why it was recalled
- Undeclared Peanuts. The firm was notified by their supplier, that the product may contain undeclared peanuts. People who are allergic to peanuts run the risk of a serious or life-threatening allergic reaction if they eat this product.
- Recall class
- Class II. Class II means the product may cause temporary or medically reversible health problems, and the chance of serious harm is remote.
- Lot codes and dates
- 1. LOT# 57221A BEST BY: 07/2026 and Lot# 56199 Best By: 07/2026 2. Lot# 57664 Best By: 07/2026
- How many
- 9,657 bottles
- Where it was sold
- Product was shipped to IL & NJ.
- Status
- Completed: the company has finished its recall actions.
- Dates
- Recall started Jun 13, 2025; FDA classified it on Oct 10, 2025; reported in FDA's enforcement report on Oct 8, 2025.
- FDA recall number
- H-0037-2026
Extract Labs, Inc. · Oct 1, 2025
- Product
- Blue Razz 20mg Gummies Brand Name: None - unlabeled bulk (private-label consignee) Generic Name: Dietary Supplement Strength: 20mg CBD and 20mg D9 THC per gummy Dosage: Not declared at bulk stage (consignee determines serving size) Form: Gummy Administration: Oral Intended use: Dietary supplement for further packaging/labeling by consignee Type of packaging: Shipped in poly gusset bags, inside corrugated brown boxes, no consumer label applied. Net wt. Blue Razz: 24 bags x 5kg and 1 bag x 4kg UPC: N/A (unlabeled bulk) Firm name & address: None (no consumer label)
- Why it was recalled
- Potential peanut protein cross-contact.
- Recall class
- Class II. Class II means the product may cause temporary or medically reversible health problems, and the chance of serious harm is remote.
- Lot codes and dates
- Lot: 25JD082307A EXP: 07/2027 Printed on bulk bag identifier adhesive
- How many
- 19,810 gummies
- Where it was sold
- Product distributed throughout the United States and Australia, Germany, United Kingdom, Malaysia, and New/Zealand.
- Status
- Terminated: FDA has closed the recall.
- Dates
- Recall started Aug 26, 2025; FDA classified it on Sep 22, 2025; reported in FDA's enforcement report on Oct 1, 2025.
- FDA recall number
- H-0623-2025
Extract Labs, Inc. · Oct 1, 2025
- Product
- Sugar-free Mixed Berry Gummies Brand Name: Extract Labs Generic Name: Dietary Supplement Strength: 10mg CBD and 10mg D9 THC per gummy Dosage: 1 gummy Form: Gummy Administration: Oral Intended use: Dietary Supplement Type of packaging: 225cc amber packer bottle with child-resistant cap and inner pressure seal Net wt: 3.53oz UPC: 850029647928 Firm name & address: Extract Labs, Inc., 1399 Horizon Ave, Lafayette, CO 80026
- Why it was recalled
- Potential peanut protein cross-contact.
- Recall class
- Class II. Class II means the product may cause temporary or medically reversible health problems, and the chance of serious harm is remote.
- Lot codes and dates
- Lot: 25E5082907A (we call this a batch ID) EXP: 07/2027 Printed on the bottom of the bottle
- How many
- 2180 gummies (109/20 ct bottles)
- Where it was sold
- Product distributed throughout the United States and Australia, Germany, United Kingdom, Malaysia, and New/Zealand.
- Status
- Terminated: FDA has closed the recall.
- Dates
- Recall started Aug 26, 2025; FDA classified it on Sep 22, 2025; reported in FDA's enforcement report on Oct 1, 2025.
- FDA recall number
- H-0621-2025
Extract Labs, Inc. · Oct 1, 2025
- Product
- Elderberry 20mg Gummies Brand Name: None - unlabeled bulk (private-label consignee) Generic Name: Dietary Supplement Strength: 20mg CBD and 20mg D9 THC per gummy Dosage: Not declared at bulk stage (consignee determines serving size) Form: Gummy Administration: Oral Intended use: Dietary supplement for further packaging/labeling by consignee Type of packaging: Shipped in poly gusset bags, inside corrugated brown boxes, no consumer label applied. Net wt. Elderberry: 24 bags x 5kg and 1 bag x 3.6kg UPC: N/A (unlabeled bulk) Firm name & address: None (no consumer label)
- Why it was recalled
- Potential peanut protein cross-contact.
- Recall class
- Class II. Class II means the product may cause temporary or medically reversible health problems, and the chance of serious harm is remote.
- Lot codes and dates
- Lot: 25JD072107A EXP: 07/2027 Printed on bulk bag identifier adhesive
- How many
- 19,720 gummies
- Where it was sold
- Product distributed throughout the United States and Australia, Germany, United Kingdom, Malaysia, and New/Zealand.
- Status
- Terminated: FDA has closed the recall.
- Dates
- Recall started Aug 26, 2025; FDA classified it on Sep 22, 2025; reported in FDA's enforcement report on Oct 1, 2025.
- FDA recall number
- H-0622-2025
Extract Labs, Inc. · Oct 1, 2025
- Product
- Mai Tai 20mg Gummies Brand Name: None - unlabeled bulk (private-label consignee) Generic Name: Dietary Supplement Strength: 20mg CBD and 20mg D9 THC per gummy Dosage: Not declared at bulk stage (consignee determines serving size) Form: Gummy Administration: Oral Intended use: Dietary supplement for further packaging/labeling by consignee Type of packaging: Shipped in poly gusset bags, inside corrugated brown boxes, no consumer label applied. Net wt. Mai Tai: 24 bags x 5kg and 1 bag x 4kg UPC: N/A (unlabeled bulk) Firm name & address: None (no consumer label)
- Why it was recalled
- Potential peanut protein cross-contact.
- Recall class
- Class II. Class II means the product may cause temporary or medically reversible health problems, and the chance of serious harm is remote.
- Lot codes and dates
- Lot: 25JD042507A EXP: 07/2027 Printed on bulk bag identifier adhesive
- How many
- 19,750 gummies
- Where it was sold
- Product distributed throughout the United States and Australia, Germany, United Kingdom, Malaysia, and New/Zealand.
- Status
- Terminated: FDA has closed the recall.
- Dates
- Recall started Aug 26, 2025; FDA classified it on Sep 22, 2025; reported in FDA's enforcement report on Oct 1, 2025.
- FDA recall number
- H-0624-2025
Abdallah Incorporated · Sep 24, 2025
- Product
- Sea Salt Caramel Dark Miniature, Item ID: 2237 ML. Packed On (YYMMDD): 25-07-22. 5.20 lb. Box. Abdallah Candies
- Why it was recalled
- Undeclared allergen (peanut, pecan). People who are allergic to peanuts run the risk of a serious or life-threatening allergic reaction if they eat this product.
- Recall class
- Class II. Class II means the product may cause temporary or medically reversible health problems, and the chance of serious harm is remote.
- Lot codes and dates
- Bulk Lot #: 5694-78645-0
- How many
- 1 box
- Where it was sold
- PA
- Status
- Terminated: FDA has closed the recall.
- Dates
- Recall started Aug 25, 2025; FDA classified it on Sep 12, 2025; reported in FDA's enforcement report on Sep 24, 2025.
- FDA recall number
- H-0580-2025
Abdallah Incorporated · Sep 24, 2025
- Product
- Cream Caramels, Milk, Item ID: 2210L. Packed On (YYMMDD): 25-06-16. 6.26 lb. Box. Abdallah Candies
- Why it was recalled
- Undeclared allergen (peanut, pecan). People who are allergic to peanuts run the risk of a serious or life-threatening allergic reaction if they eat this product.
- Recall class
- Class II. Class II means the product may cause temporary or medically reversible health problems, and the chance of serious harm is remote.
- Lot codes and dates
- Bulk Lot #: 5679-75157-0
- How many
- 1 box
- Where it was sold
- PA
- Status
- Terminated: FDA has closed the recall.
- Dates
- Recall started Aug 25, 2025; FDA classified it on Sep 12, 2025; reported in FDA's enforcement report on Sep 24, 2025.
- FDA recall number
- H-0581-2025
The Candy Barn · Sep 10, 2025
- Product
- Grandma's Old-Fashioned Peanut Brittle, The Candy Barn, 1113 Palm Ave Riverside, IA 52327, Net Wt: 4oz, flexible plastic bag
- Why it was recalled
- Allergen labeling: missing allergens (peanuts, milk) in contains statement
- Recall class
- Class II. Class II means the product may cause temporary or medically reversible health problems, and the chance of serious harm is remote.
- Lot codes and dates
- No coding
- How many
- 665 packages Total
- Where it was sold
- Stringtown Grocery, Kalona, IA Golden Delight Bakery, Kalona, IA
- Status
- Terminated: FDA has closed the recall.
- Dates
- Recall started Aug 6, 2025; FDA classified it on Sep 3, 2025; reported in FDA's enforcement report on Sep 10, 2025.
- FDA recall number
- H-0566-2025
The Candy Barn · Sep 10, 2025
- Product
- Chocolate Fudge, The Candy Barn, 1113 Palm Ave Riverside, IA 52327, Net Wt: 4oz, 10oz, packed in plastic clamshell
- Why it was recalled
- Allergen labeling: egg is not listed in the 'contains' statement
- Recall class
- Class II. Class II means the product may cause temporary or medically reversible health problems, and the chance of serious harm is remote.
- Lot codes and dates
- No coding
- How many
- 665 packages Total
- Where it was sold
- Stringtown Grocery, Kalona, IA Golden Delight Bakery, Kalona, IA
- Status
- Terminated: FDA has closed the recall.
- Dates
- Recall started Aug 6, 2025; FDA classified it on Sep 3, 2025; reported in FDA's enforcement report on Sep 10, 2025.
- FDA recall number
- H-0559-2025
The Candy Barn · Sep 10, 2025
- Product
- Maple Nut Fudge, The Candy Barn, 1113 Palm Ave Riverside, IA 52327, Net Wt: 4oz, 10oz, packed in plastic clamshell
- Why it was recalled
- Allergen labeling: specific tree nut (pecan) and egg not listed in 'contains' statement
- Recall class
- Class II. Class II means the product may cause temporary or medically reversible health problems, and the chance of serious harm is remote.
- Lot codes and dates
- No coding
- How many
- 665 packages Total
- Where it was sold
- Stringtown Grocery, Kalona, IA Golden Delight Bakery, Kalona, IA
- Status
- Terminated: FDA has closed the recall.
- Dates
- Recall started Aug 6, 2025; FDA classified it on Sep 3, 2025; reported in FDA's enforcement report on Sep 10, 2025.
- FDA recall number
- H-0564-2025
The Candy Barn · Sep 10, 2025
- Product
- English Toffee, The Candy Barn, 1113 Palm Ave Riverside, IA 52327, Net Wt: 5oz, packed in flexible plastic bag
- Why it was recalled
- Allergen labeling: specific tree nut (pecans) not listed in the 'contains' statement
- Recall class
- Class II. Class II means the product may cause temporary or medically reversible health problems, and the chance of serious harm is remote.
- Lot codes and dates
- No coding
- How many
- 665 packages Total
- Where it was sold
- Stringtown Grocery, Kalona, IA Golden Delight Bakery, Kalona, IA
- Status
- Terminated: FDA has closed the recall.
- Dates
- Recall started Aug 6, 2025; FDA classified it on Sep 3, 2025; reported in FDA's enforcement report on Sep 10, 2025.
- FDA recall number
- H-0565-2025
The Candy Barn · Sep 10, 2025
- Product
- Peanut Butter Fudge, The Candy Barn, 1113 Palm Ave Riverside, IA 52327, Net Wt: 4oz, 10oz, packed in plastic clamshell
- Why it was recalled
- Allergen labeling: egg not listed in the 'contains' statement
- Recall class
- Class II. Class II means the product may cause temporary or medically reversible health problems, and the chance of serious harm is remote.
- Lot codes and dates
- No coding
- How many
- 665 packages Total
- Where it was sold
- Stringtown Grocery, Kalona, IA Golden Delight Bakery, Kalona, IA
- Status
- Terminated: FDA has closed the recall.
- Dates
- Recall started Aug 6, 2025; FDA classified it on Sep 3, 2025; reported in FDA's enforcement report on Sep 10, 2025.
- FDA recall number
- H-0563-2025
The Candy Barn · Sep 10, 2025
- Product
- Chocolate Walnut Fudge, The Candy Barn, 1113 Palm Ave Riverside, IA 52327, Net Wt: 4oz, 10oz, packed in plastic clamshell
- Why it was recalled
- Allergen labeling: specific tree nut (walnut) and egg are not listed in the 'contains' statement
- Recall class
- Class II. Class II means the product may cause temporary or medically reversible health problems, and the chance of serious harm is remote.
- Lot codes and dates
- No coding
- How many
- 665 packages Total
- Where it was sold
- Stringtown Grocery, Kalona, IA Golden Delight Bakery, Kalona, IA
- Status
- Terminated: FDA has closed the recall.
- Dates
- Recall started Aug 6, 2025; FDA classified it on Sep 3, 2025; reported in FDA's enforcement report on Sep 10, 2025.
- FDA recall number
- H-0560-2025
The Candy Barn · Sep 10, 2025
- Product
- Chocolate Mint Fudge, The Candy Barn, 1113 Palm Ave Riverside, IA 52327, Net Wt: 4oz, 10oz, packed in plastic clamshell
- Why it was recalled
- Allergen labeling: egg is not listed in the 'contains' statement
- Recall class
- Class II. Class II means the product may cause temporary or medically reversible health problems, and the chance of serious harm is remote.
- Lot codes and dates
- No coding
- How many
- 665 packages Total
- Where it was sold
- Stringtown Grocery, Kalona, IA Golden Delight Bakery, Kalona, IA
- Status
- Terminated: FDA has closed the recall.
- Dates
- Recall started Aug 6, 2025; FDA classified it on Sep 3, 2025; reported in FDA's enforcement report on Sep 10, 2025.
- FDA recall number
- H-0561-2025
The Candy Barn · Sep 10, 2025
- Product
- Pecan Toffee Clusters, The Candy Barn, 1113 Palm Ave Riverside, IA 52327, Net Wt: 5oz, flexible plastic bag
- Why it was recalled
- Allergen labeling: specific tree nut (pecan) not listed in 'contains' statement
- Recall class
- Class II. Class II means the product may cause temporary or medically reversible health problems, and the chance of serious harm is remote.
- Lot codes and dates
- No coding
- How many
- 665 packages Total
- Where it was sold
- Stringtown Grocery, Kalona, IA Golden Delight Bakery, Kalona, IA
- Status
- Terminated: FDA has closed the recall.
- Dates
- Recall started Aug 6, 2025; FDA classified it on Sep 3, 2025; reported in FDA's enforcement report on Sep 10, 2025.
- FDA recall number
- H-0567-2025
The Candy Barn · Sep 10, 2025
- Product
- Chocolate Pecan Fudge, The Candy Barn, 1113 Palm Ave Riverside, IA 52327, Net Wt: 4oz, 10oz, packed in plastic clamshell
- Why it was recalled
- Allergen labeling: specific tree nut (pecan) and egg are not listed in the 'contains' statement
- Recall class
- Class II. Class II means the product may cause temporary or medically reversible health problems, and the chance of serious harm is remote.
- Lot codes and dates
- No coding
- How many
- 665 packages Total
- Where it was sold
- Stringtown Grocery, Kalona, IA Golden Delight Bakery, Kalona, IA
- Status
- Terminated: FDA has closed the recall.
- Dates
- Recall started Aug 6, 2025; FDA classified it on Sep 3, 2025; reported in FDA's enforcement report on Sep 10, 2025.
- FDA recall number
- H-0562-2025
Reisman Bros Bakery · Aug 6, 2025
- Product
- Reisman's Candy Blast Brownie Snack 3 oz.
- Why it was recalled
- Undeclared wheat People who are allergic to wheat, or who have celiac disease, run the risk of a serious reaction if they eat this product.
- Recall class
- Class II. Class II means the product may cause temporary or medically reversible health problems, and the chance of serious harm is remote.
- Lot codes and dates
- UPC: 078619010574
- How many
- 186,582 units (total)
- Where it was sold
- NY, NJ, PA, MD, IL, CA, FL, MA, MI
- Status
- Terminated: FDA has closed the recall.
- Dates
- Recall started Jun 17, 2025; FDA classified it on Jul 31, 2025; reported in FDA's enforcement report on Aug 6, 2025.
- FDA recall number
- H-0378-2025
DANONE US LLC · Jul 23, 2025
- Product
- YoCrunch Low Fat Yogurt with Toppers, Strawberry with milk chocolate M&Ms minis candies, Packaged in the following size containers: 1. Single Serve Cup, 6 oz. (170g) UPC 46675-00083 2. Multipack containing 4-4 oz. cups UPC 46675-01312 Keep Refrigerated. Distributed by Danone US, LLC, White Plains, NY 10605
- Why it was recalled
- Foreign material (plastic pieces) Pieces of foreign material in food can cause injuries such as cuts to the mouth or choking.
- Recall class
- Class II. Class II means the product may cause temporary or medically reversible health problems, and the chance of serious harm is remote.
- Lot codes and dates
- Lot # / Expiration Date: 1. 2025.07.12, 2025.07.25, 2025.08.07, 2025.08.22, 2025.09.04 2. 2025.07.08, 2025.07.12, 2025.07.13, 2025.07.17, 2025.07.18, 2025.07.26, 2025.07.27, 2025.08.02, 2025.08.03, 2025.08.09, 2025.08.11, 2025.08.12, 2025.08.13, 2025.08.15, 2025.08.16, 2025.08.23, 2025.08.24, 2025.08.29, 2025.08.30, 2025.08.31
- How many
- 2,492,073 cases (total)
- Where it was sold
- Nationwide
- Status
- Terminated: FDA has closed the recall.
- Dates
- Recall started Jul 11, 2025; FDA classified it on Jul 17, 2025; reported in FDA's enforcement report on Jul 23, 2025.
- FDA recall number
- H-0300-2025
Rich Ice Cream Co · Jul 23, 2025
- Product
- Cotton Candy Twirl Bar (86260), stick novelties 2.5 FL. Oz (74mL)., Individually packaged in a plastic bag. Master case that consists of 4 packers with 24 units in each packer, total 96 units in a master case. Keep Frozen.
- Why it was recalled
- Potential Listeria Monocytogenes Contamination Listeria monocytogenes can cause serious and sometimes fatal infections in young children, frail or elderly people and others with weakened immune systems. Healthy people may have short-term symptoms such as high fever, severe headache, stiffness, nausea, abdominal pain and diarrhea. Listeria infection can cause miscarriages and stillbirths.
- Recall class
- Class II. Class II means the product may cause temporary or medically reversible health problems, and the chance of serious harm is remote.
- Lot codes and dates
- Lot # 24351 through lot # 25156 (Julian calendar)
- How many
- Total of 110,292 cases to include all products
- Where it was sold
- Distributed to: CA, PA, OH, GA, NY, NJ, FL, TX, VA, AZ, AL, IL, MO, MA, TN, IA, SC, OR, OK, NV, LA, WI, NE, Nassau, Bahamas
- Status
- Terminated: FDA has closed the recall.
- Dates
- Recall started Jun 27, 2025; FDA classified it on Jul 17, 2025; reported in FDA's enforcement report on Jul 23, 2025.
- FDA recall number
- H-0290-2025
Vita Warehouse Corp. · Jul 9, 2025
- Product
- 1. Welby Vitamin B12 Adult Gummies 140 Count 2. Berkely Jensen¿ Vitamin B12 1000 mcg Gummies 250 count 3. VitaGlobe" Vitamin B12 Extra Strength Gummies 140 count 3. Vita Labs Vitamin B-12 Gummies Bulk 500 count
- Why it was recalled
- Contains undeclared peanut People who are allergic to peanuts run the risk of a serious or life-threatening allergic reaction if they eat this product.
- Recall class
- Class I. Class I is FDA's most serious category: a reasonable chance that eating or using the product will cause serious health problems or death.
- Lot codes and dates
- 1. UPC Code: 4099100290868 Lot #: 248046601 Expiration Date: 10/2026 2. UPC Code: 888670132487 Lot #: 248046601 Expiration Date: 10/2026 3. UPC Code: 850005214670 Lot #: 248046601 Expiration Date: 10/2026 4. Lot# 248046601 Expiration date: 10/2026
- How many
- 40,522 bottles plus 582,000 individual gummies
- Where it was sold
- Nationwide
- Status
- Terminated: FDA has closed the recall.
- Dates
- Recall started Jun 11, 2025; FDA classified it on Jul 3, 2025; reported in FDA's enforcement report on Jul 9, 2025.
- FDA recall number
- H-0212-2025
NEW GRAINS GLUTEN FREE BAKERY · Jun 11, 2025
- Product
- Frosted Sugar Cookie: Gluten-free frosted sugar cookies, clear plastic bag, 4 oz, 6 cookies/package Ingredients: White rice flour, Powdered sugar, Butter, Sugar, Palm shortening, Sprinkles, Rice milk, Egg whites, Potato flour, Imitation vanilla, Baking powder, Xanthan gum, Gelatin, Salt, Red dye. Frosting: Powdered sugar, Butter, Palm Fruit Oil, Rice Milk, Vanilla, Red Dye (Water, Propylene glycol, Red #40, Red #3, Yellow #6, Yellow #5). Sprinkles: Sugar, Corn Starch, Confectioner s Glaze, Yellow #5, Red #40, Carnauba wax, Red #3, Blue #1, Soy Ingredients. Contains: Soy, Egg whites, Milk ingredients
- Why it was recalled
- Due to printing quality, label does not declare these allergens clearly: Egg, Milk, Soy.
- Recall class
- Class I. Class I is FDA's most serious category: a reasonable chance that eating or using the product will cause serious health problems or death.
- Lot codes and dates
- Affected products do not have legible lot codes due to the labeling issue. The print quality on the packaging rendered lot and date codes unreadable or missing entirely.
- How many
- Approximately 50 units
- Where it was sold
- Utah
- Status
- Terminated: FDA has closed the recall.
- Dates
- Recall started Apr 23, 2025; FDA classified it on May 30, 2025; reported in FDA's enforcement report on Jun 11, 2025.
- FDA recall number
- F-0832-2025
Nordic Naturals, Inc. · Jun 11, 2025
- Product
- Nordic Naturals Zero Sugar Kids Multivitamin Supplement - Gummies (120 gummies/bottle); 12 bottles/case
- Why it was recalled
- Product is mislabeled.
- Recall class
- Class III. Class III is FDA's lowest-risk category: the product is not likely to cause health problems.
- Lot codes and dates
- Lot: 244423 RUS-30127 Expiration 05/2026
- How many
- 1164 bottles (120 gummies/bottle)
- Where it was sold
- Domestic: AK, AZ, CA, CO, FL, GA, ID, IN, MA, MT, NC, ND, NH, NV, NY, OK, OR, RI, UT, WA; Foreign: Great Britain, UAE
- Status
- Terminated: FDA has closed the recall.
- Dates
- Recall started May 2, 2025; FDA classified it on Jun 3, 2025; reported in FDA's enforcement report on Jun 11, 2025.
- FDA recall number
- F-0840-2025
Wells Enterprises, Inc. · May 21, 2025
- Product
- Cotton Candy Flavored Ice Cream, 3 GAL, Wells Enterprises, INC dba Wells Dairy, Inc Le Mars, IA 51031, UPC: 070640050482, Item: 662429
- Why it was recalled
- Foreign material (plastic) may be present in ice cream product Pieces of foreign material in food can cause injuries such as cuts to the mouth or choking.
- Recall class
- Class II. Class II means the product may cause temporary or medically reversible health problems, and the chance of serious harm is remote.
- Lot codes and dates
- Jet Code: 3G BB PREM COTTON CANDY IC 1CS LOT50018 HH 19115 18:00 5099 BEST IF USED BY 10/08/26
- How many
- 39 3-gallon tubs
- Where it was sold
- 103 distribution centers across the US
- Status
- Terminated: FDA has closed the recall.
- Dates
- Recall started Apr 25, 2025; FDA classified it on May 14, 2025; reported in FDA's enforcement report on May 21, 2025.
- FDA recall number
- F-0784-2025
Blooming Import Inc. · Apr 23, 2025
- Product
- Golden Crop Candy (10 oz. (283g) wrapped candies)
- Why it was recalled
- Contains undeclared and unallowed colors (Blue 1, Red 40, Acid Red 18)
- Recall class
- Class II. Class II means the product may cause temporary or medically reversible health problems, and the chance of serious harm is remote.
- Lot codes and dates
- UPC Code: 73476513450
- How many
- 74 cases total
- Where it was sold
- NY, PA, MD, NJ, MA, MO, DE, TX
- Status
- Terminated: FDA has closed the recall.
- Dates
- Recall started Mar 5, 2025; FDA classified it on Apr 16, 2025; reported in FDA's enforcement report on Apr 23, 2025.
- FDA recall number
- F-0716-2025
Blooming Import Inc. · Apr 23, 2025
- Product
- Golden Crop Candy (8 oz. (227g) un-wrapped candies)
- Why it was recalled
- Contains undeclared and unallowed colors (Blue 1, Red 40, Acid Red 18)
- Recall class
- Class II. Class II means the product may cause temporary or medically reversible health problems, and the chance of serious harm is remote.
- Lot codes and dates
- UPC Code: 734765134587
- How many
- 74 cases total
- Where it was sold
- NY, PA, MD, NJ, MA, MO, DE, TX
- Status
- Terminated: FDA has closed the recall.
- Dates
- Recall started Mar 5, 2025; FDA classified it on Apr 16, 2025; reported in FDA's enforcement report on Apr 23, 2025.
- FDA recall number
- F-0717-2025
Tristar Food Wholesale Co Inc · Apr 23, 2025
- Product
- BaiWei ShanZhuang, Dried Seedless Plum Candy, 9.16 oz. (260g), plastic bags, 30 bags per case.
- Why it was recalled
- Product contains cyclamates
- Recall class
- Class III. Class III is FDA's lowest-risk category: the product is not likely to cause health problems.
- Lot codes and dates
- Lot: 04162026 BC 6937218914734
- How many
- 50 Cartons
- Where it was sold
- The recalled product was distributed to the following states: MA, NY, MI, FL, TX, IA, IL, CO, NE, RI, WI,
- Status
- Terminated: FDA has closed the recall.
- Dates
- Recall started Mar 4, 2025; FDA classified it on Apr 11, 2025; reported in FDA's enforcement report on Apr 23, 2025.
- FDA recall number
- F-0705-2025
Mauna Loa Macadamia Nut Company, LLC · Mar 19, 2025
- Product
- Mauna Loa Milk Chocolate Covered Macadamias product is a snack product and packaged in plastic 1oz pouch. Each carton contains 12 pouches, and each master case contains 12 cartons. Retail Pouch (1oz pouch) UPC: 0 72992 04260 3 Carton (12 pouches) UPC: 72992 04261 Master Case (12 cartons/12 pouches) UPC: 72992 04262 The ingredients statement declares: Milk Chocolate (Sugar, Cocoa Butter, Milk, Chocolate, Soy Lecithin (emulsifier), Vanilla), Dry Roasted Macadamia Nuts, Powdered Sugar (Sugar, Corn Starch), Maltodextrin, Confectionary Glaze, Sugar. CONTAINS: Tree nuts (Macadamia), Milk, and Soy.
- Why it was recalled
- Undeclared almonds People who are allergic to tree nuts run the risk of a serious or life-threatening allergic reaction if they eat this product.
- Recall class
- Class I. Class I is FDA's most serious category: a reasonable chance that eating or using the product will cause serious health problems or death.
- Lot codes and dates
- Retail 1oz pouch has lot code K4351 C2 and BB 07 2026
- How many
- 74 cases (each case contains 12 cartons/12/1oz. pouches)
- Where it was sold
- Distributed in CA and MI.
- Status
- Terminated: FDA has closed the recall.
- Dates
- Recall started Feb 14, 2025; FDA classified it on Mar 13, 2025; reported in FDA's enforcement report on Mar 19, 2025.
- FDA recall number
- F-0636-2025
Health and Happiness (H&H) LLC. · Mar 12, 2025
- Product
- Biostime Kids Calm & Sleep Support Fruity Bites Probiotics and Prebiotics Fiber Sachets (gummies), Flexible Sachet packaging, Sample size package (4 Count), EXP: JUL/2025 Lot : 2413352PSF
- Why it was recalled
- Due to foreign object: metal balls (tiny non-magnetic metal balls measuring less than 2mm inside the gummies) intended for children Pieces of foreign material in food can cause injuries such as cuts to the mouth or choking.
- Recall class
- Class II. Class II means the product may cause temporary or medically reversible health problems, and the chance of serious harm is remote.
- Lot codes and dates
- EXP: JUL/2025 Lot : 2413352PSF
- How many
- 125,000 free samples (total)
- Where it was sold
- Distributed in the US: IL, TN, CA
- Status
- Terminated: FDA has closed the recall.
- Dates
- Recall started Jan 17, 2025; FDA classified it on Feb 28, 2025; reported in FDA's enforcement report on Mar 12, 2025.
- FDA recall number
- F-0584-2025
The Candy Basket Inc · Feb 19, 2025
- Product
- Marionberry Jelly Sticks DARK, item number CB745-D, is packed and sold in bulk 4lbs. boxes. Product does not have a UPC and is not repackaged for retail. Product was sold out of bulk chocolate cases from candy stores to consumers without any labeling. Label on bulk 4lbs. box declares as "Ingredients: Dark Chocolate (***milk fat (butter)***soya lecithin), Sugar, Corn Syrup, Fruit Pectin,***Vegetable Oil". Manufactured By: The Candy Basket, Inc. Portland, OR.
- Why it was recalled
- Undeclared Red #3, Blue #1, Potassium Sorbate, and Propylene Glycol.
- Recall class
- Class III. Class III is FDA's lowest-risk category: the product is not likely to cause health problems.
- Lot codes and dates
- All lots up to 025014.
- How many
- 516/4lb. boxes total
- Where it was sold
- distributed in CA, OR and WA.
- Status
- Terminated: FDA has closed the recall.
- Dates
- Recall started Jan 15, 2025; FDA classified it on Feb 13, 2025; reported in FDA's enforcement report on Feb 19, 2025.
- FDA recall number
- F-0560-2025
The Candy Basket Inc · Feb 19, 2025
- Product
- Orange Jelly Sticks DARK, item number CB741-D, is packed and sold in bulk 4lbs. boxes. Product does not have a UPC and is not repackaged for retail. Product was sold out of bulk chocolate cases from candy stores to consumers without any labeling. Label on bulk 4lbs. box declares "Ingredients: Dark Chocolate (***milk fat (butter), soya lecithin***), Sugar, Corn Syrup, Fruit Pectin,***Vegetable Oil". Manufactured By: The Candy Basket, Inc. Portland, OR.
- Why it was recalled
- Undeclared Yellow #6, and Sodium Benzoate.
- Recall class
- Class II. Class II means the product may cause temporary or medically reversible health problems, and the chance of serious harm is remote.
- Lot codes and dates
- All lots up to 025014.
- How many
- 516/4lb. boxes total
- Where it was sold
- distributed in CA, OR and WA.
- Status
- Terminated: FDA has closed the recall.
- Dates
- Recall started Jan 15, 2025; FDA classified it on Feb 13, 2025; reported in FDA's enforcement report on Feb 19, 2025.
- FDA recall number
- F-0556-2025
The Candy Basket Inc · Feb 19, 2025
- Product
- Lemon Jelly Sticks WHITE, item number CB750-W, is packed and sold in bulk 4lbs. boxes. Product does not have a UPC and is not repackaged for retail. Product was sold out of bulk chocolate cases from candy stores to consumers without any labeling. Label on bulk 4lbs. box declares "Ingredients: White Chocolate (***whey, nonfat milk***soya lecithin), Sugar, Corn Syrup, Fruit Pectin,***Vegetable Oil". Manufactured By: The Candy Basket, Inc. Portland, OR.
- Why it was recalled
- Undeclared Yellow #5 and Potassium Sorbate.
- Recall class
- Class II. Class II means the product may cause temporary or medically reversible health problems, and the chance of serious harm is remote.
- Lot codes and dates
- All lots up to 025014.
- How many
- 516/4lb. boxes total
- Where it was sold
- distributed in CA, OR and WA.
- Status
- Terminated: FDA has closed the recall.
- Dates
- Recall started Jan 15, 2025; FDA classified it on Feb 13, 2025; reported in FDA's enforcement report on Feb 19, 2025.
- FDA recall number
- F-0558-2025
The Candy Basket Inc · Feb 19, 2025
- Product
- Lemon Jelly Sticks DARK, item number CB750-D, is packed and sold in bulk 4lbs. boxes. Product does not have a UPC and is not repackaged for retail. Product was sold out of bulk chocolate cases from candy stores to consumers without any labeling. Label on bulk 4lbs. box declares "Ingredients: Dark Chocolate (***milk fat (butter), soya lecithin***), Sugar, Corn Syrup, Fruit Pectin,***Vegetable Oil". Manufactured By: The Candy Basket, Inc. Portland, OR.
- Why it was recalled
- Undeclared Yellow #5 and Potassium Sorbate.
- Recall class
- Class II. Class II means the product may cause temporary or medically reversible health problems, and the chance of serious harm is remote.
- Lot codes and dates
- All lots up to 025014.
- How many
- 516/4lb. boxes total
- Where it was sold
- distributed in CA, OR and WA.
- Status
- Terminated: FDA has closed the recall.
- Dates
- Recall started Jan 15, 2025; FDA classified it on Feb 13, 2025; reported in FDA's enforcement report on Feb 19, 2025.
- FDA recall number
- F-0557-2025
The Candy Basket Inc · Feb 19, 2025
- Product
- Marionberry Jelly Sticks MILK, item number CB745-M, is packed and sold in bulk 4lbs. boxes. Product does not have a UPC and is not repackaged for retail. Product was sold out of bulk chocolate cases from candy stores to consumers without any labeling. Label on bulk 4lbs. box declares as "Ingredients: Milk Chocolate (***milk***soya lecithin), Sugar, Corn Syrup, Fruit Pectin,***Vegetable Oil". Manufactured By: The Candy Basket, Inc. Portland, OR.
- Why it was recalled
- Undeclared Red #3, Blue #1, Potassium Sorbate, and Propylene Glycol.
- Recall class
- Class III. Class III is FDA's lowest-risk category: the product is not likely to cause health problems.
- Lot codes and dates
- All lots up to 025014.
- How many
- 516/4lb. boxes total
- Where it was sold
- distributed in CA, OR and WA.
- Status
- Terminated: FDA has closed the recall.
- Dates
- Recall started Jan 15, 2025; FDA classified it on Feb 13, 2025; reported in FDA's enforcement report on Feb 19, 2025.
- FDA recall number
- F-0559-2025
The Candy Basket Inc · Feb 19, 2025
- Product
- Orange Jelly Sticks MILK, item number CB741-M, is packed and sold in bulk 4lbs. boxes. Product does not have a UPC and is not repackaged for retail. Product was sold out of bulk chocolate cases from candy stores to consumers without any labeling. Label on bulk 4lbs. box declares "Ingredients: Milk Chocolate (***soya lecithin***), Sugar, Corn Syrup, Fruit Pectin, ***Vegetable Oil". Manufactured By: The Candy Basket, Inc. Portland, OR.
- Why it was recalled
- Undeclared Yellow #6, and Sodium Benzoate.
- Recall class
- Class II. Class II means the product may cause temporary or medically reversible health problems, and the chance of serious harm is remote.
- Lot codes and dates
- All lots up to 025014.
- How many
- 516/4lb. boxes total
- Where it was sold
- distributed in CA, OR and WA.
- Status
- Terminated: FDA has closed the recall.
- Dates
- Recall started Jan 15, 2025; FDA classified it on Feb 13, 2025; reported in FDA's enforcement report on Feb 19, 2025.
- FDA recall number
- F-0555-2025
The Candy Basket Inc · Feb 19, 2025
- Product
- Raspberry Jelly Sticks DARK, Item Number CB747-D, packed and sold in bulk 4lbs. boxes. Product does not have a UPC and is not repackaged for retail. Product was sold out of bulk chocolate cases from candy stores to consumers without any labeling. Label on bulk 4lbs. box declares as "Ingredients: Dark Chocolate (***milk fat (butter)***soya lecithin), Sugar, Corn Syrup, Fruit Pectin,***Vegetable Oil". Manufactured By: The Candy Basket, Inc. Portland, OR.
- Why it was recalled
- Undeclared Red #40 and Potassium Sorbate
- Recall class
- Class III. Class III is FDA's lowest-risk category: the product is not likely to cause health problems.
- Lot codes and dates
- All lots up to 025014.
- How many
- 516/4lb. boxes total
- Where it was sold
- distributed in CA, OR and WA.
- Status
- Terminated: FDA has closed the recall.
- Dates
- Recall started Jan 15, 2025; FDA classified it on Feb 13, 2025; reported in FDA's enforcement report on Feb 19, 2025.
- FDA recall number
- F-0562-2025
The Candy Basket Inc · Feb 19, 2025
- Product
- Raspberry Jelly Sticks MILK, item number CB747-M, is packed and sold in bulk 4lbs. boxes. Product does not have a UPC and is not repackaged for retail. Product was sold out of bulk chocolate cases from candy stores to consumers without any labeling. Label on bulk 4lbs. box declares as "Ingredients: Milk Chocolate (***milk***soya lecithin), Sugar, Corn Syrup, Fruit Pectin,***Vegetable Oil". Manufactured By: The Candy Basket, Inc. Portland, OR.
- Why it was recalled
- Undeclared Red #40 and Potassium Sorbate.
- Recall class
- Class III. Class III is FDA's lowest-risk category: the product is not likely to cause health problems.
- Lot codes and dates
- All lots up to 025014.
- How many
- 516/4lb. boxes total
- Where it was sold
- distributed in CA, OR and WA.
- Status
- Terminated: FDA has closed the recall.
- Dates
- Recall started Jan 15, 2025; FDA classified it on Feb 13, 2025; reported in FDA's enforcement report on Feb 19, 2025.
- FDA recall number
- F-0561-2025
GARDNER'S CANDIES , INC · Jan 8, 2025
- Product
- Gardner's Candies Cappuccino Meltaway Bar 1.25 oz. (35g), Item Number: 15207/online website item number is 0015207, sold individually and; also as part of Gardner's Meltaway Treat Box 6 oz, Item Number: 50135 or online website item number is 0050135
- Why it was recalled
- Product contains Undeclared Allergen Tree Nuts (Cashews) People who are allergic to tree nuts run the risk of a serious or life-threatening allergic reaction if they eat this product.
- Recall class
- Class I. Class I is FDA's most serious category: a reasonable chance that eating or using the product will cause serious health problems or death.
- Lot codes and dates
- Gardner's Cappuccino Meltaway Bar: dated 082725; Gardner's Meltaway Treat Box: dated either 101625 or 112525
- How many
- 2,007 bars. 196 of the bars went into the Meltaway Treat boxes.
- Where it was sold
- The recalled product was distributed to the following States: PA, OH, GA, MN, NM, MD, KY, SC, FL, MO, CA
- Status
- Terminated: FDA has closed the recall.
- Dates
- Recall started Dec 10, 2024; FDA classified it on Jan 2, 2025; reported in FDA's enforcement report on Jan 8, 2025.
- FDA recall number
- F-0376-2025
Yoder's Cashew Crunch · Dec 25, 2024
- Product
- Hard candy packed in clear plastic bag with gold/red label, Yoder's Cashew Crunch, 14oz, 2620 Hwy. 22, Riverside, IA 52327
- Why it was recalled
- Undeclared allergen labeling (milk) People who are allergic or sensitive to milk run the risk of a serious or life-threatening allergic reaction if they eat this product.
- Recall class
- Class II. Class II means the product may cause temporary or medically reversible health problems, and the chance of serious harm is remote.
- Lot codes and dates
- No coding system in place
- How many
- 32 packages; 28 lbs.
- Where it was sold
- Distributed to retail and wholesale in: IA and GA
- Status
- Terminated: FDA has closed the recall.
- Dates
- Recall started Nov 4, 2024; FDA classified it on Dec 16, 2024; reported in FDA's enforcement report on Dec 25, 2024.
- FDA recall number
- F-0294-2025
Yoder's Cashew Crunch · Dec 25, 2024
- Product
- Yoder's Cashew Crunch Corn, bulk candy coated popcorn packaged in clear plastic without label.
- Why it was recalled
- Undeclared allergen labeling (milk) People who are allergic or sensitive to milk run the risk of a serious or life-threatening allergic reaction if they eat this product.
- Recall class
- Class II. Class II means the product may cause temporary or medically reversible health problems, and the chance of serious harm is remote.
- Lot codes and dates
- No coding system in place
- How many
- 138.92 pounds
- Where it was sold
- Distributed to retail and wholesale in: IA and GA
- Status
- Terminated: FDA has closed the recall.
- Dates
- Recall started Nov 4, 2024; FDA classified it on Dec 16, 2024; reported in FDA's enforcement report on Dec 25, 2024.
- FDA recall number
- F-0297-2025
Yoder's Cashew Crunch · Dec 25, 2024
- Product
- Candy coated popcorn packaged in clear plastic with gold label, 7 oz, Yoders Cashew Crunch Corn, 2620 Hwy. 22, Riverside, IA 52327
- Why it was recalled
- Undeclared allergen labeling (milk) People who are allergic or sensitive to milk run the risk of a serious or life-threatening allergic reaction if they eat this product.
- Recall class
- Class II. Class II means the product may cause temporary or medically reversible health problems, and the chance of serious harm is remote.
- Lot codes and dates
- No coding system in place
- How many
- 319 packages; 139 lbs.
- Where it was sold
- Distributed to retail and wholesale in: IA and GA
- Status
- Terminated: FDA has closed the recall.
- Dates
- Recall started Nov 4, 2024; FDA classified it on Dec 16, 2024; reported in FDA's enforcement report on Dec 25, 2024.
- FDA recall number
- F-0296-2025
Yoder's Cashew Crunch · Dec 25, 2024
- Product
- Yoder's Cashew Crunch, hard candy shipped in bulk in clear plastic bag.
- Why it was recalled
- Undeclared allergen labeling (milk) People who are allergic or sensitive to milk run the risk of a serious or life-threatening allergic reaction if they eat this product.
- Recall class
- Class II. Class II means the product may cause temporary or medically reversible health problems, and the chance of serious harm is remote.
- Lot codes and dates
- No coding system in place
- How many
- 384.12 pounds
- Where it was sold
- Distributed to retail and wholesale in: IA and GA
- Status
- Terminated: FDA has closed the recall.
- Dates
- Recall started Nov 4, 2024; FDA classified it on Dec 16, 2024; reported in FDA's enforcement report on Dec 25, 2024.
- FDA recall number
- F-0295-2025
Yoder's Cashew Crunch · Dec 25, 2024
- Product
- Hard candy packed in clear plastic bag with gold/red label, Yoder's Cashew Crunch, Wt. 7oz, 2620 Hwy. 22, Riverside, IA 52327
- Why it was recalled
- Undeclared allergen labeling (milk) People who are allergic or sensitive to milk run the risk of a serious or life-threatening allergic reaction if they eat this product.
- Recall class
- Class II. Class II means the product may cause temporary or medically reversible health problems, and the chance of serious harm is remote.
- Lot codes and dates
- No coding system in place
- How many
- 435 packages; 190 lbs.
- Where it was sold
- Distributed to retail and wholesale in: IA and GA
- Status
- Terminated: FDA has closed the recall.
- Dates
- Recall started Nov 4, 2024; FDA classified it on Dec 16, 2024; reported in FDA's enforcement report on Dec 25, 2024.
- FDA recall number
- F-0293-2025
What to do
- Compare the brand, product name, size, UPC and the lot code or best-by date on your package with the recall. Recalls usually cover specific lots or dates, not every package.
- If your product matches, do not eat it. Return it to the store for a refund or throw it away, as the recall notice says.
- If you or someone in your family feels sick after eating a recalled food, call your doctor and say which product it was. Get emergency care for severe symptoms.
- Report a problem or illness to FDA through the Safety Reporting Portal (safetyreporting.hhs.gov). For meat, poultry and egg products, call USDA at 1-888-674-6854.