Undeclared fish or shellfish food recalls: brands, lot codes and what to do
Short answer: FDA has listed 21 Undeclared fish or shellfish food 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.
About Undeclared fish or shellfish: People who are allergic to fish or shellfish run the risk of a serious or life-threatening allergic reaction if they eat this product. (FDA's standard recall-notice wording.)
Search all FDA food recalls by product, brand, UPC or lot code.
All 21 recalls
Recall details
El Ruisenor De Mexico, Inc. · Oct 28, 2026
- Product
- Dried Cod; packed in a clear plastic bag. 1lb, 5lb, 50lb unit size. No UPC
- Why it was recalled
- undeclared allergen ingredient (Fish) People who are allergic to fish or shellfish run the risk of a serious or life-threatening allergic reaction if they eat this product.
- 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: 440024553-11-001
- How many
- 102 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-0111-2027
El Ruisenor De Mexico, Inc. · Oct 28, 2026
- Product
- Ground Shrimp; packed in a clear plastic 1lb, 5lb, 25-50lb unit sizes. No UPC
- Why it was recalled
- undeclared allergen ingredient (shrimp) People who are allergic to fish or shellfish run the risk of a serious or life-threatening allergic reaction if they eat this product.
- 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
- no lot code
- How many
- 263.52 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-0115-2027
El Ruisenor De Mexico, Inc. · Oct 28, 2026
- Product
- Dried Whole Shrimp; packed in a clear plastic 1lb, 5lb, 30lb unit sizes. No UPC
- Why it was recalled
- undeclared allergen ingredient (shrimp) People who are allergic to fish or shellfish run the risk of a serious or life-threatening allergic reaction if they eat this product.
- 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
- no lot code
- How many
- 192 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-0114-2027
TOJI CO. · Oct 7, 2026
- Product
- Cloud Cafe branded Collagen Milk; Strawberry Milk Zero; Caffeine Free; 10pc/box
- Why it was recalled
- Undeclared allergen ingredient (fish) People who are allergic to fish or shellfish 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
- OB25001; Best By: 5/13/2028
- How many
- 820 boxes
- Where it was sold
- Product was sold to a single distributor located in Los Angeles.
- Status
- Ongoing: the recall is still active.
- Dates
- Recall started Sep 15, 2026; FDA classified it on Sep 29, 2026; reported in FDA's enforcement report on Oct 7, 2026.
- FDA recall number
- H-1400-2026
Pacific Health Sciences Llc · Oct 7, 2026
- Product
- Organiccs Absolutely Pure, Type-1 Hydrolyzed Collagen Peptides, All-Natural Aid for Strengthening Hair, Skin, Nails, Muscles & Joints, 180 Veggie Capsules. UPC: none
- Why it was recalled
- Undeclared shellfish (crab shell): source of ingredient Glucosamine sulfate People who are allergic to fish or shellfish 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
- 25009CP
- How many
- 395 units
- Where it was sold
- Product is primarily distributed to private practice medical offices in California, Oregon, Washington, Kentucky, Massachusetts, and Hawaii
- Status
- Ongoing: the recall is still active.
- Dates
- Recall started Sep 14, 2026; FDA classified it on Sep 29, 2026; reported in FDA's enforcement report on Oct 7, 2026.
- FDA recall number
- H-1401-2026
GELLERT GLOBAL GROUP · Jul 29, 2026
- Product
- Fusia, Asian Inspirations, Kimchi & Tofu Kimbap, 8.1 OZ (230 g), Paper Film Wrapper, 12 packages per case , 6 ea: Kimchi & Tofu Kimbap / 6 ea Spicy Tuna with Gochujang Kimbap, Keep Frozen-Do Not Thaw .
- Why it was recalled
- Undeclared Allergen (Fish) People who are allergic to fish or shellfish 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
- Best if Used By: October 8, 2027
- How many
- 29,850 units
- Where it was sold
- The adulterated product was distributed to the following states: NY, PA, CT, NC, TX, MD
- Status
- Ongoing: the recall is still active.
- Dates
- Recall started Jun 25, 2026; FDA classified it on Jul 23, 2026; reported in FDA's enforcement report on Jul 29, 2026.
- FDA recall number
- H-1186-2026
Azuma Foods International Inc USA · Jun 24, 2026
- Product
- azuma foods TAKO WASABI Seasoned Octopus with Wasabi PERISHABLE/KEEP FROZEN PRODUCT OF JAPAN DISTRIBUTED BY: AZUMA FOODS INTERNATIONAL INC., U.S.A. HAYWARD, CA 94545 Retail: 3-50g PACKS NET WT. 5.3 OZ (150g) UPC: 745329900647 Foodservice: 2.2lbs UPC: 745329900746
- Why it was recalled
- Undeclared fish. People who are allergic to fish or shellfish 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 - lot code, best by date: 1CFFDA2, 11/20/2026; 1CFGCH2, 12/18/2026; 1CFIBC2, 2/2/2027; 1CFJCG2, 3/19/2027; 1CFKBH2, 4/9/2027; 1CGBAH2, 6/30/2027. Foodservice - lot code, best by date: 1CFFCI2, 11/18/2026; 1CFFCJ2, 11/19/2026; 1CFFCJ2, 11/29/2026; 1CFFDA2, 11/20/2026; 1CFGCA2, 12/11/2026; 1CFGCA2, 12/11/2026; 1CFGCG2, 12/17/2026; 1CFGCH2, 12/18/2026; 1CFHBB2, 1/1/2027; 1CFIBC2, 2/2/2027; 1CFICI2, 2/18/2027; 1CFICJ2, 2/19/2027; 1CFJAF2, 2/26/2026; 1CFJCG2, 3/19/2027; 1CFKBG2, 4/8/2027; 1CFKBH2, 4/9/2027; 1CFKBH2, 4/9/2027; 1CFLAH2, 4/30/2027; 1CFLCJ2, 5/22/2027; 1CGBAH2, 6/30/2027; 1CGBBE2, 7/7/2027; 1CGBBE2, 7/7/2027; 1CGBCC2, 7/15/2027; 1CGBCC2, 7/15/2027; 1CGBCD2, 7/16/2027.
- How many
- Retail: 545 cases (12 3-pack units/case); Foodservice: 3616 cases (12 units/case)
- Where it was sold
- Domestic: AK, AZ, CA, CO, FL, GA, HI, IL, MD, MA, NC, NJ, NV, NY, OR, TX, WA
- Status
- Ongoing: the recall is still active.
- Dates
- Recall started May 28, 2026; FDA classified it on Jun 18, 2026; reported in FDA's enforcement report on Jun 24, 2026.
- FDA recall number
- H-1075-2026
Kettle Cuisine, LLC · Jun 17, 2026
- Product
- Individual Unit Label (both lid and front of cup): Whole Foods Market Kitchens Minestrone Soup, VEGETARIAN NET WT 24 OZ (1 Lb 8OZ) 680g. Case Label: Whole Foods Global Minestrone Soup 702505, KEEP REFRIGERATED, Distributed by Whole Foods Market Austin, TX 78703. Eight (8)/ 24 oz. Cups (Net Wt. 12 LBS)/case.
- Why it was recalled
- Contains undeclared allergen (shrimp). People who are allergic to fish or shellfish 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
- Use by: 05/27/26 Lot/Unit Numbers: 1762181 UPC Codes: 099482502065
- How many
- 562 cases (4,496 - 24oz units)
- Where it was sold
- AL, CT, DC, FL, GA, MA, MD, ME, MS, NC, NH, NJ, NY, PA, RI, SC, TN, VA
- Status
- Ongoing: the recall is still active.
- Dates
- Recall started May 19, 2026; FDA classified it on Jun 10, 2026; reported in FDA's enforcement report on Jun 17, 2026.
- FDA recall number
- H-0941-2026
Ocinet, Inc. · May 20, 2026
- Product
- ...And Kimchi branded kimchi; packaged in 3 sizes of glass containers (126oz, 63oz, 30oz); 126oz UPC- 8541200408 62oz UPC- 8651200409 30oz UPC- 8541200411
- Why it was recalled
- Undeclared allergen ingredient (fish) People who are allergic to fish or shellfish 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 lot numbers provided. Recall includes all product.
- How many
- 199,750 units (across 3 different sizes)
- Where it was sold
- Product was distributed to locations in California, Texas and Georgia.
- Status
- Terminated: FDA has closed the recall.
- Dates
- Recall started May 1, 2026; FDA classified it on May 14, 2026; reported in FDA's enforcement report on May 20, 2026.
- FDA recall number
- H-0780-2026
Perfect Pasta, Incorporated · Mar 11, 2026
- Product
- Lobster & Crab Ravioli. Keep Frozen. Contains: Wheat, Eggs, Milk, Crustaceans-Shellfish. Product is intended to be further cooked. Weight: 1-10 pound (4.5g). Use within 6 months. 801-541-9292-www.FunarosPerfectPasta.com. 1391 So. 300 West Slc, Ut 84115.
- Why it was recalled
- Undeclared shrimp, crab, lobster, pollock (fish), whiting (fish), and soy. People who are allergic to soy 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
- Made on: JAN 19 2026
- How many
- 42/ 10 lb cases
- Where it was sold
- Distributed to consignees in Utah only.
- Status
- Terminated: FDA has closed the recall.
- Dates
- Recall started Feb 8, 2026; FDA classified it on Mar 24, 2026; reported in FDA's enforcement report on Mar 11, 2026.
- FDA recall number
- H-0620-2026
Reser's Fine Foods, Inc. · Feb 25, 2026
- Product
- The Tuna Salad product container is mislabeled with a Chicken Salad lid, which states: Molly Kitchen's Chicken Salad, 789953, NET WT. 5 LB (2.26 kg) per plastic tub. UPC 7 5810830149 8. Distributed by US Foods, Inc. Rosemont, IL 60018. The lid declares Contains: Eggs, Milk, Wheat. The immediate 5-lb tub has no side labeling (besides the lid). The master cardboard case label is correct and states: Molly Kitchen's Tuna Salad, (item #) 794599, 2/5 LB tubs per case, Net Wt. 10 LB (4.53 kg). UPC 075810876447. Distributed by US Foods, Inc. Rosemont, IL 60018. Contains: Egg, Wheat, Fish (Tuna).
- Why it was recalled
- Undeclared fish allergen (tuna). Tuna Salad was mislabeled as Chicken Salad. People who are allergic to fish or shellfish 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 1410100754 Use By FEB/21/26
- How many
- 149 cases (2 tubs /case) or 298 total tubs
- Where it was sold
- Distributed in AZ, CA, NV, UT and WA.
- Status
- Terminated: FDA has closed the recall.
- Dates
- Recall started Jan 30, 2026; FDA classified it on Feb 19, 2026; reported in FDA's enforcement report on Feb 25, 2026.
- FDA recall number
- H-0517-2026
Anthony's BBQ · Jan 28, 2026
- Product
- Anthony's Barbecue & Dip-It Sauce, 15 oz. (425g) glass bottle, UPC 6 89076 62272 1. Anthony's BBQ Sauce PO Box 3239 Harbor, OR 97415. The ingredients statement on the recalled bottle is declared as "***Ingredients: Tomatoes, Brown Sugar, Distilled Water, Distilled Vinegar, Garlic, Onion, Liquid Smoke, Salt, Mustard Seed, Natural Flavor, Corn syrup, Turmeric, Paprika, Pepper, Hydrolyzed soy protein, Caramel color, 1/10 of 1% Benzoate of Soda***.
- Why it was recalled
- Undeclared allergen (fish). Anthony's Barbecue & Dip-It Sauce label does not declare Worcestershire (Anchovy). People who are allergic to fish or shellfish 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
- None
- How many
- 192/15 oz glass bottles
- Where it was sold
- Distributed only in OR.
- Status
- Terminated: FDA has closed the recall.
- Dates
- Recall started Nov 7, 2025; FDA classified it on Jan 16, 2026; reported in FDA's enforcement report on Jan 28, 2026.
- FDA recall number
- H-0407-2026
WFM Purchasing, LP · Jan 21, 2026
- Product
- Brussel Sprouts & Kale Slaw
- Why it was recalled
- Undeclared Fish and Egg Allergen People who are allergic to eggs 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
- No code
- How many
- 88 units
- Where it was sold
- New York, New Jersey and Virginia
- Status
- Terminated: FDA has closed the recall.
- Dates
- Recall started Dec 31, 2025; FDA classified it on Jan 14, 2026; reported in FDA's enforcement report on Jan 21, 2026.
- FDA recall number
- H-0403-2026
Plenus Group Inc. · Nov 26, 2025
- Product
- Rockport Lobser Bisque; packed in 2x8lb pouches and in 4x4b pouches
- Why it was recalled
- Products contain undeclared shrimp (crustacean shellfish) People who are allergic to fish or shellfish 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
- a. 2x8lb pouch with Production Date: 09/05/2025, MFG Code: 25248, Best By Date: 03/06/2027, Lot Number: 069161 b. 2x8lb pouch with Production Date: 09/05/2025, MFG Code: 25248, Best By Date: 03/06/2027, Lot Number: 069162 c. 2x8lb pouch with Production Date: 09/11/2025, MFG Code: 25254, Best By Date: 03/12/2027, Lot Number: 069321 d. 2x8lb pouch with Production Date: 09/11/2025; MFG Code: 25254, Best By Date: 03/12/2025, Lot Number 069322 e. 4x4lb pouch with Production Date: 09/12/2025, MFG Code: 25255, Best By Date: 03/13/2027, Lot Number: 069323 f. 2x8lb pouch with Production Date: 09/30/2025, MFG Code: 25273, Best By Date: 03/31/2027, Lot Number: 070042 g. 2x8lb pouch with Production Date: 09/30/2025, MFG Code: 25273, Best By Date: 03/31/2027, Lot Number: 070043 h. 4x4lb pouch with Production Date: 09/30/2025, MFG Code: 25273, Best By Date: 03/31/2027, Lot Number: 070064
- How many
- 130 cases (product code 4031) and 529 cases (product code 2031)
- Where it was sold
- Massachusetts, Michigan, New Hampshire, Vermont, Illinois, Florida, Pennsylvania, Rhode Island. Tennessee, and Puerto Rico (US Territory)
- Status
- Terminated: FDA has closed the recall.
- Dates
- Recall started Oct 29, 2025; FDA classified it on Nov 19, 2025; reported in FDA's enforcement report on Nov 26, 2025.
- FDA recall number
- H-0201-2026
New York Mutual Trading, Inc. · Nov 12, 2025
- Product
- Frozen Crab Paste; 3.5 OZ (100g); Imported by Mutual Tading Co. Inc. UPC# 72546723040 "Not for retail Sale" Frozen Crab Paste IM-2 in w/Tray; 500g; Imported by Mutual Trading Co. Inc. UPC# 72546607852 "Not for retail Sale" Frozen Crab Paste; 17.6 OZ (500g); Imported by Mutual Tading Co. Inc. UPC# 72546607852 "Not for retail Sale"
- Why it was recalled
- Undeclared allergen ingredients (fish, soy, and 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 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
- Expiration Dates for 3.5 oz: 2025.11.10; 2026.02.09; 2026.03.09; 2026.05.26; 2026.06.20 Expiration Dates for 500g: 2026.05.12
- How many
- ~ 21 cases across both recalled products
- Where it was sold
- Products were labeled "not for retail sale" and were distributed to various restaurants across HI, FL, GA, MA, MD, NJ, NY, PA.
- Status
- Terminated: FDA has closed the recall.
- Dates
- Recall started Oct 3, 2025; FDA classified it on Oct 31, 2025; reported in FDA's enforcement report on Nov 12, 2025.
- FDA recall number
- H-0147-2026
Tai Foong USA Inc · Nov 5, 2025
- Product
- Fusia Asian Inspirations brand Veggie Spring Rolls. Net weight: 10 oz (283.5 g).) retail package identified by UPC 4099100222258. Type of packaging: Paperboard carton with inner poly bag; 12 ct corrugated master case. Responsible firm on label: ALDI Inc. Batavia, IL 60510 (U.S. private label).
- Why it was recalled
- Undeclared shrimp People who are allergic to fish or shellfish 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 code: 70961125137, Best Before 05/17/2027
- How many
- 1,261 cases (12 boxes per case)
- Where it was sold
- Distributed in AL, CT, DC, DE, FL, GA, LA, MA, MD, MS, NC, NH, NJ, NY, OK, PA, RI, SC, TN, TX, VA, VT, and WV.
- Status
- Terminated: FDA has closed the recall.
- Dates
- Recall started Oct 8, 2025; FDA classified it on Oct 28, 2025; reported in FDA's enforcement report on Nov 5, 2025.
- FDA recall number
- H-0143-2026
ONE FROZEN, LLC · Oct 22, 2025
- Product
- Good and Gather brand Southwest-Style Burrito Bowl Blend Processed in a facility that also handles shellfish, egg, fish, milk, sesame, soy, tree nut and wheat ingredients
- Why it was recalled
- Product may contain undeclared shrimp (crustacean shellfish). People who are allergic to fish or shellfish 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: 5505-1 and 5505-2
- How many
- 57,240 bags
- Where it was sold
- Nationwide.
- Status
- Terminated: FDA has closed the recall.
- Dates
- Recall started Sep 4, 2025; FDA classified it on Oct 10, 2025; reported in FDA's enforcement report on Oct 22, 2025.
- FDA recall number
- H-0042-2026
Lee K of NY Inc. · Oct 15, 2025
- Product
- PINOCCHIO CATERING Aged Kimchi Mackerel; 57oz; 27330700000 in black bottomed plastic container
- Why it was recalled
- Product contains undeclared milk and shrimp 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 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
- Expiration dates prior to 09/16/25.
- How many
- 43 units
- Where it was sold
- NY and NJ
- Status
- Terminated: FDA has closed the recall.
- Dates
- Recall started Sep 8, 2025; FDA classified it on Oct 7, 2025; reported in FDA's enforcement report on Oct 15, 2025.
- FDA recall number
- H-0024-2026
GNC Holdings LLC · Jun 11, 2025
- Product
- GNC Women's 30+ Vitapak, Carton of 30 Sachets. Each sachet contains four tablets and a capsule. Paper-board carton that measures 10.25 width x 3.56 height x 3.15 depth containing 30 sachets of 3 width x 2.75 height with tear notch. 15 Cartons per Case
- Why it was recalled
- Undeclared Fish allergen (parvalbumin). People who are allergic to fish or shellfish run the risk of a serious or life-threatening allergic reaction if they eat this product.
- 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 No. 1060EB2401 1060EB2402 1060EB2403 1060EB2404 1060EB2405 1060EB2501 1060EB2502 1060EB2503
- How many
- 144,430 Units
- Where it was sold
- The adulterated product was distributed to the various states: AL, AR, AZ, CA, CO, CT, DC, DE, FL, GA, HI, IA, ID, IL, IN, KS, KY, LA, MA, MD, ME, MI, MN, MO, MS, NC, ND, NE, NH, NJ, NM, NV, NY, OH, OK, OR, PA, PR, RI, SC, TN, TX, UT, VA, WA, WI, WV, WY
- Status
- Terminated: FDA has closed the recall.
- Dates
- Recall started Apr 25, 2025; FDA classified it on Jun 5, 2025; reported in FDA's enforcement report on Jun 11, 2025.
- FDA recall number
- F-0928-2025
Borsari Food Company Inc · Jan 1, 2025
- Product
- BORSARI Food Company Incorporated; BLOODY MARY MIX ; 32 FL. OZ; INGREDIENTS: Tomato juice, corn syrup, non-fat milk solids, orange juice, lemon juice, lime juice, cayenne pepper, vinegar, salt, garlic powder, Worcestershire sauce, prepared horseradish, maltic acid, sodium and potassium benzoate, yellow 5 & 6; UPC: 815893000101
- Why it was recalled
- Product contains undeclared fish (anchovy) and soy. People who are allergic to soy 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
- All products within expiry.
- How many
- 5,818 units
- Where it was sold
- AL, AZ, CA, CT, FL, GA, IL, IN, KS, MA, MD, MI, MN, MT, NM, NY, OH, PA, RI, SC, SD, TN, UT, VA, WA
- Status
- Terminated: FDA has closed the recall.
- Dates
- Recall started Dec 9, 2024; FDA classified it on Dec 24, 2024; reported in FDA's enforcement report on Jan 1, 2025.
- FDA recall number
- F-0317-2025
SE Tampa Inc dba Tampa Food · Dec 25, 2024
- Product
- Crab Cheese Rangoon, NET WT: 8 LB, 120 pieces of 30g / 3 Trays per master cardboard boxes, Keep Frozen, packaged in corrugated cardboard box.
- Why it was recalled
- Undeclared allergens: Milk, Soy, Crustacea Shellfish, Fish 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 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#2411311, 2411312, 2411317, 2411318 Expiration Date: April 2025
- How many
- 191 cases
- Where it was sold
- FL
- Status
- Terminated: FDA has closed the recall.
- Dates
- Recall started Nov 25, 2024; FDA classified it on Dec 18, 2024; reported in FDA's enforcement report on Dec 25, 2024.
- FDA recall number
- F-0299-2025
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.