Baby and toddler food recalls: brands, lot codes and what to do
Short answer: FDA has listed 21 baby and toddler food recalls reported since November 2024; the most recent was reported on Oct 28, 2026 (Pacific Health Sciences Llc). 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 21 recalls
Recall details
Pacific Health Sciences Llc · Oct 28, 2026
- Product
- Babies' Magic Tea; Baby Sleep Gripe Water; Dietary Supplement; Net Wt. 4 OZ; Age 2eeks+ "No Alcohol, Dairy, Wheat, Soy And Animal Testing" UPC: 850302008183
- Why it was recalled
- Adulterated (elevated levels of alcohol) infant dietary supplement
- 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: 25122bw Expiration date: 12/2028
- How many
- 953 units
- Where it was sold
- Product was manufactured for a single customer located in Florida. Product was made available through Amazon and through the customers website.
- Status
- Ongoing: the recall is still active.
- Dates
- Recall started Oct 6, 2026; FDA classified it on Oct 21, 2026; reported in FDA's enforcement report on Oct 28, 2026.
- FDA recall number
- H-0168-2027
NARA ORGANICS INC · Jul 8, 2026
- Product
- a.) nara organics brand; Whole Milk Organic Infant Formula; Milk-based Powder with Iron; 0-12 months; NET WT 24.7 OZ (700 G); UPC: 860013251901 b.) nara organics brand; Whole Milk Organic Infant Formula; Milk-based Powder with Iron; 0-12 months; NET WT 14.1 OZ (400 G); UPC: 860013251918
- Why it was recalled
- Product may be contaminated with Clostridium botulinum. Clostridium botulinum can cause botulism, a serious and potentially fatal illness. Symptoms can include blurred or double vision, drooping eyelids, slurred speech, trouble swallowing or breathing and muscle weakness.
- 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
- Recalled Lot Codes - 408125075E14F2 - 708125076E14F2 - 708125083E14F2 - 408125139E14F2 - 708125141E14F2 - 708125145E14F2 - 708125174E14F2 - 709125273E14F2 - 709125280E14F2 - 709125288E14F2 - 409125307E14F2 - 70926019ENNB - 70926029ENNB - 70926035ENNB - 70926039ENNB - 70926042ENNB Use-By dates span March 16, 2027 - February 11, 2028
- How many
- 377,610 cans
- Where it was sold
- nationwide
- Status
- Ongoing: the recall is still active.
- Dates
- Recall started Jun 13, 2026; FDA classified it on Jul 1, 2026; reported in FDA's enforcement report on Jul 8, 2026.
- FDA recall number
- H-1137-2026
The a2 Milk Company · Jun 10, 2026
- Product
- a2 Platinum Premium infant formula Milk-based Powder with Iron 31.7oz (900g) Intended use: infant formula (0 12 months). Condition: shelf stable product Type of packaging: metal tin with plastic dust cap. Net weight: 31.7oz (900gm). UPC: 813267020335. Firm name listed on label: The a2 Milk Company. 4909 Pearl East Circle, Suite 300 Boulder CO 80301.
- Why it was recalled
- Possible contamination with Cereulide toxin.
- 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 # 2210321712 with Expiration Date: 01/14/2027, Lot # 2210324609 with Expiration Date 01/21/2027, Lot # 2210269454 with Expiration Date 07/15/2026
- How many
- 51,202 units
- Where it was sold
- The recalled product was distributed throughout the United States.
- Status
- Terminated: FDA has closed the recall.
- Dates
- Recall started May 1, 2026; FDA classified it on May 29, 2026; reported in FDA's enforcement report on Jun 10, 2026.
- FDA recall number
- H-0891-2026
IF Holding II, LLC · Mar 11, 2026
- Product
- tippy toes apple pear banana 6 months & up baby food 2-4OZ (113g) PACKS NET WT 8 OZ (226g) DISTRIBUTED BY TOPCO ASSOCIATES LLC ELK GROVE VILLAGE, IL 60007 1-888-423-0139 PRODUCT OF USA UPC: 036800265783
- Why it was recalled
- Potential contamination with patulin.
- 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: 07174 BB: 07/17/2026
- How many
- 1375 cases
- Where it was sold
- U.S. Consignees: IL
- Status
- Ongoing: the recall is still active.
- Dates
- Recall started Feb 5, 2026; FDA classified it on Mar 5, 2026; reported in FDA's enforcement report on Mar 11, 2026.
- FDA recall number
- H-0544-2026
Valley Springs Artesian Gold, LLC · Mar 4, 2026
- Product
- Valley Springs 100% Natural Bottled Water packaged in the following size plastic jug with plastic caps: 1. 1 Gal Net 128 Fl oz. UPC 0 31193-00701 9. Bottled by Valley Springs/Artesian Gold, LLC, Portage WI 53901. 2. 2.5 Gallon Net (320 Fl oz./9.4L). UPC 0 31193-01501 4. Bottled by Valley Springs/Artesian Gold, LLC, Portage WI 53901. 3. Infant Water, 1 Gal Net, 128 FL. Oz. Not sterile. Use as directed by physician or by labeling directions for use of infant formula. UPC 0 31193-01401 7. 4. Daisy's Doggy Water, 1 Gal Net, 128 FL. Oz. 100% Pure Water. No Chlorine. UPC 0 31193-90100 3. Bottled by Valley Springs/Artesian Gold, LLC, Portage WI 53901. Distributed by DDW LLC, 109 S. Thompson Rd., Sun Prairie, WI 53590.
- Why it was recalled
- Water was bottled under insanitary conditions.
- 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
- How many
- 379,868 units
- Where it was sold
- IL, WI
- Status
- Ongoing: the recall is still active.
- Dates
- Recall started Feb 6, 2026; FDA classified it on Feb 26, 2026; reported in FDA's enforcement report on Mar 4, 2026.
- FDA recall number
- H-0534-2026
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
A New Life Herbs, LLC · Dec 31, 2025
- Product
- Baby Soothe Herbal Supplement, Promotes rest, helps ease colic, upset stomach, and teething discomfort, Contains: Catnip, Chamomile, Vegetable Glycerin, water; packaged in a 2 oz. glass dropper bottle
- Why it was recalled
- Unapproved drug claims on product labeling and product misbranded due to no Supplement Facts label
- 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
- E164BS EXP 1/27 E128BS EXP 7/26
- How many
- 49 bottles
- Where it was sold
- AL, AZ, CA, GA, IL, IN, MN, MO, MS, NC, NY, TN
- Status
- Terminated: FDA has closed the recall.
- Dates
- Recall started Nov 20, 2025; FDA classified it on Dec 23, 2025; reported in FDA's enforcement report on Dec 31, 2025.
- FDA recall number
- H-0342-2026
A New Life Herbs, LLC · Dec 31, 2025
- Product
- Baby Allergy Herbal Supplement, Contains: Echinacea Purpurea, Oregon Grape Root, Dandelion & Burdock Root, Fenugreek, Ginger Root in vegetable glycerin; packaged in a 2 oz. glass dropper bottle, UPC 249953949282
- Why it was recalled
- Unapproved drug claims on product labeling and product misbranded due to no Supplement Facts label
- 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
- E166SA EXP 4/28
- How many
- 23 bottles
- Where it was sold
- AL, AZ, CA, GA, IL, IN, MN, MO, MS, NC, NY, TN
- Status
- Terminated: FDA has closed the recall.
- Dates
- Recall started Nov 20, 2025; FDA classified it on Dec 23, 2025; reported in FDA's enforcement report on Dec 31, 2025.
- FDA recall number
- H-0341-2026
CHETAK NEW YORK LLC · Dec 17, 2025
- Product
- Deep-brand Premium Select Baby Bhindi KEEP FROZEN Net Wt. 12 oz (340 g)
- Why it was recalled
- Product tested positive Salmonella . Salmonella can cause serious and sometimes fatal infections in young children, frail or elderly people and others with weakened immune systems. Healthy people may have fever, diarrhea (which may be bloody), nausea, vomiting and abdominal pain.
- 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: 24536, 25007, 25035, 25053, 25078, 25081, 25132, 25163, 25193
- How many
- 3509532 bags
- Where it was sold
- United States
- Status
- Terminated: FDA has closed the recall.
- Dates
- Recall started Sep 5, 2025; FDA classified it on Dec 11, 2025; reported in FDA's enforcement report on Dec 17, 2025.
- FDA recall number
- H-0251-2026
ByHeart, INC. · Dec 17, 2025
- Product
- 1. ByHeart Whole Nutrition Infant Formula cans 24 OZ 680 grams; Cans sold in 1 pack, 2 packs, 4 packs, or 6 packs 2. ByHeart Whole Nutrition Infant Formula Anywhere Packs Single Serve Packet 17 grams in packages containing 14 Single Serve Packets
- Why it was recalled
- Contaminated with Clostridium botulinum Clostridium botulinum can cause botulism, a serious and potentially fatal illness. Symptoms can include blurred or double vision, drooping eyelids, slurred speech, trouble swallowing or breathing and muscle weakness.
- 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
- All batches and codes within expiry Finished Product Quantity 08NOV2023 to 08NOV2025 UPC Codes: Single Can: 8 50044 96800 8; Sams Club 2PK: 00850044968893; Amazon 2PK: 00850044968053; Anywhere pack: 8 50044 96802 2; 1-Count Sample Unit Anywhere Pack: 850044968015
- How many
- 3,482,131 Cans and 3,531,901 Single Serve Packets.
- Where it was sold
- nationwide
- Status
- Ongoing: the recall is still active.
- Dates
- Recall started Nov 8, 2025; FDA classified it on Dec 10, 2025; reported in FDA's enforcement report on Dec 17, 2025.
- FDA recall number
- H-0249-2026
M.O.M Enterprises, LLC. · Oct 15, 2025
- Product
- Organic BABY bedtime drops; sleep + immunity blend; Promotes restful sleep with natural herbs & supports immunity with elderberry & vitamin C; LIQUID DIETARY SUPPLEMENT; AGE 4 MONTHS+, NET WT. 2 OZ (60 ML)
- Why it was recalled
- Potential yeast contamination.
- 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 code: 25100, 25148, 25155 UPC: 679234051814 EXP 04/2027, 05/2027, 06/2027
- How many
- 46,752 units/bottles (Lot 25100: 8,424 units; Lot 25148: 16,488 units; Lot 25155: 21,840 units)
- Where it was sold
- AL, AR, AZ, CA, CO, CT, DE, FL, GA, IA, IL, IN, KS, KY, LA, MI, MN, MO, MS, NC, ND, NH, NJ, NY, OH, OR, PA, SC, TN, TX, UT, VA, WI
- Status
- Ongoing: the recall is still active.
- Dates
- Recall started Sep 12, 2025; FDA classified it on Oct 7, 2025; reported in FDA's enforcement report on Oct 15, 2025.
- FDA recall number
- H-0025-2026
M.O.M Enterprises, LLC. · Sep 17, 2025
- Product
- Organic BABY bedtime drops; sleep + immunity blend; Promotes restful sleep with natural herbs & supports immunity with elderberry & vitamin C; LIQUID DIETARY SUPPLEMENT; AGE 4 MONTHS+, NET WT. 2 OZ (60 ML)
- Why it was recalled
- Potential for spoilage due to yeast contamination.
- 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 code: 25084; 25086; UPC: 679234051814 EXP 03/2027
- How many
- 85,248 units/bottles (Lot 25084: 51,096 units; Lot 25086: 34,152 units)
- Where it was sold
- AL, AR, AZ, CA, CO, CT, FL, GA, IA, IL, IN, KS, KY, MI, MN, MO, MS, NC, ND, NJ, NV, NY, OH, OR, PA, RI, SC, TN, TX, VA, WI
- Status
- Ongoing: the recall is still active.
- Dates
- Recall started Aug 5, 2025; FDA classified it on Sep 8, 2025; reported in FDA's enforcement report on Sep 17, 2025.
- FDA recall number
- H-0576-2025
UNFI General Corporate · Jul 16, 2025
- Product
- 1. USA ORGC BOK CHOY 2. USA/MEX OG2 BABY BOKCHOY
- Why it was recalled
- May be contaminated with fluid from a reach truck
- 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. UPC: 00-78783-90734 case code: 204 2. UPC: 03-72500-69952 case code: 69951
- How many
- 213 cases (total)
- Where it was sold
- NJ, NY, MD, DC, PA
- Status
- Terminated: FDA has closed the recall.
- Dates
- Recall started Jun 7, 2025; FDA classified it on Jul 10, 2025; reported in FDA's enforcement report on Jul 16, 2025.
- FDA recall number
- H-0235-2025
JFE FRANCHISING INC · Jul 9, 2025
- Product
- Fruit & Vegetable Tray - 64 oz 63912394047 Mixed Melon, Cucumbers & Tajin - 18oz 63912394007 Watermelon & Cucumber w/ Tajin - 18oz 63912394036 Small Vegetable Tray - 19.5 oz 63912388045 Small Party Tray with Dip - 19 oz 63912388046 Large Vegetable Tray - 42 oz 63912388056 Vegetable Bowl - 26 oz 63912388044 Vegetable Bowl - 13 oz 63912388072 Baby Carrot, Cucumber, & Ranch - 15 oz 63912394045 Signature Vegetable Bowl - 28 oz 639123600172
- Why it was recalled
- Cucumbers have the potential to be contaminated with Salmonella. Salmonella can cause serious and sometimes fatal infections in young children, frail or elderly people and others with weakened immune systems. Healthy people may have fever, diarrhea (which may be bloody), nausea, vomiting and abdominal pain.
- 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
- Sell by 5/20/2025
- How many
- unknown
- Where it was sold
- AL, IL, IN, KY, MI, TN, WI
- Status
- Ongoing: the recall is still active.
- Dates
- Recall started May 20, 2025; FDA classified it on Jul 1, 2025; reported in FDA's enforcement report on Jul 9, 2025.
- FDA recall number
- H-0207-2025
Publix Super Markets, Inc. · Jun 11, 2025
- Product
- Greenwise Pear Kiwi Spinach & Pea Baby Food Pouch. Net Wt 4 oz. (113g). Stage 2 6 months+, Best if" date of 11/01/2025. Packed in 14 pouches per case, 4 oz per pouch. Distributed by Publix Super Markets, Inc. 3300 Publix Corporate Parkway Lakeland, FL 33881.
- Why it was recalled
- Elevated levels of Lead, cadmium and arsenic Lead is toxic. Exposure can cause serious health effects, especially in children.
- 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 Code 24BA306 best-used-by date of 11-01-2025 Global Trade Item Number is 41414-00901
- How many
- 53620 units equaling 3830 cases
- Where it was sold
- FL, GA, SC, NC, TN, AL, VA, KY
- Status
- Terminated: FDA has closed the recall.
- Dates
- Recall started May 9, 2025; FDA classified it on Jun 3, 2025; reported in FDA's enforcement report on Jun 11, 2025.
- FDA recall number
- H-0005-2025
FRUSELVA USA · Apr 9, 2025
- Product
- Good & Gather baby Pea, Zucchini, Kale & Thyme Vegetable Puree. Net Wt 4 oz. (113g). 6+ months. UPC 1 91907-99314 1. Distributed by Target Corporation, Minneapolis, MN 55403. Product of Colombia
- Why it was recalled
- elevated level of lead Lead is toxic. Exposure can cause serious health effects, especially in children.
- 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: 4169, Best by Dec 09 2025, Lot Number: 4167, Best by Dec 07 2025.
- How many
- 25,600 units
- Where it was sold
- Nationwide
- Status
- Terminated: FDA has closed the recall.
- Dates
- Recall started Mar 12, 2025; FDA classified it on Apr 3, 2025; reported in FDA's enforcement report on Apr 9, 2025.
- FDA recall number
- F-0693-2025
Nestle-USA, Inc. (Corporate Office) · Mar 5, 2025
- Product
- Gerber Snacks for Baby Soothe 'n' Chew TEETHING STICKS Banana NET WT 3.2 OZ (90g) box UPC 0 15000 04608 8 and NET WT 1.59 oz box UPC 0 15000 01015 7 GERBER PRODUCTS CO., FREMONT, MI 49413
- Why it was recalled
- Firm received complaints of infant choking.
- 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
- All lots
- How many
- 34,652cs/5/1.59 oz boxes + 271,115cs/5/3.2 oz boxes
- Where it was sold
- The products were shipped to distribution centers in the following states: AL, AR, AZ, CA, CO, CT, DE, FL, GA, HI, IA, ID, IL, IN, KS, KY, LA, MA, MD, ME, MI, MN, MO, MS, MT, NC, NE, NH, NJ, NV, NY, OH, OK, OR, PA, RI, SC, SD, TN, TX, UT, VA, VT, WA, WI and Puerto Rico.
- Status
- Terminated: FDA has closed the recall.
- Dates
- Recall started Jan 31, 2025; FDA classified it on Feb 25, 2025; reported in FDA's enforcement report on Mar 5, 2025.
- FDA recall number
- F-0579-2025
Nestle-USA, Inc. (Corporate Office) · Mar 5, 2025
- Product
- Gerber Snacks for Baby Soothe 'n' Chew TEETHING STICKS Strawberry Apple NET WT 3.2 OZ (90g) UPC 0 15000 04518 7 GERBER PRODUCTS CO., FREMONT, MI 49413
- Why it was recalled
- Firm received complaints of infant choking.
- 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
- All lots
- How many
- 314,398cs/5/3.2 oz boxes
- Where it was sold
- The products were shipped to distribution centers in the following states: AL, AR, AZ, CA, CO, CT, DE, FL, GA, HI, IA, ID, IL, IN, KS, KY, LA, MA, MD, ME, MI, MN, MO, MS, MT, NC, NE, NH, NJ, NV, NY, OH, OK, OR, PA, RI, SC, SD, TN, TX, UT, VA, VT, WA, WI and Puerto Rico.
- Status
- Terminated: FDA has closed the recall.
- Dates
- Recall started Jan 31, 2025; FDA classified it on Feb 25, 2025; reported in FDA's enforcement report on Mar 5, 2025.
- FDA recall number
- F-0578-2025
Grimmway Enterprises, Inc. dba Grimmway Farms · Jan 8, 2025
- Product
- --- Organic Baby Carrots --- Organic Baby Carrots 25 Grimmway Farms; Organic Baby Carrots 25 Lbs. Grimmway Farms --- Brand --- Grimmway Farms
- Why it was recalled
- Potential contamination with E. coli O121:H19 Some E. coli strains, such as O157:H7, can cause bloody diarrhea and abdominal cramps, and some people develop a type of kidney failure called hemolytic uremic syndrome (HUS).
- 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
- 127734 127773 127830 127871 127875 127936 127975 127978 128036 128059 128063 128129 128133 128163 128238 128264 128291 128336 128383 128482
- How many
- 21,094 cases
- Where it was sold
- Distribution Centers located in U.S. States: AL, AR, AZ, CA, CO, CT, FL, GA, HI, IA, ID, IL, IN, KS, KY, LA, MA, MD, MI, MN, MO, NC, NH, NJ, NM, NV, NY, OH, OK, OR, PA, RI, SC, TN, TX, UT, VA, VT, WA, WI U.S. Territories: Puerto Rico Foreign Countries: Canada, United Arab Emirates, Hong Kong, Columbia
- Status
- Terminated: FDA has closed the recall.
- Dates
- Recall started Nov 16, 2024; FDA classified it on Dec 31, 2024; reported in FDA's enforcement report on Jan 8, 2025.
- FDA recall number
- F-0359-2025
Grimmway Enterprises, Inc. dba Grimmway Farms · Jan 8, 2025
- Product
- --- Organic Baby Carrots --- Organic Baby Peeled Carrots 12/12oz Steam-to-Serve; Organic Baby Peel Carrot12/12oz Steam-to-Serve RPC --- Brand --- Cal-Organic; Marketside
- Why it was recalled
- Potential contamination with E. coli O121:H19 Some E. coli strains, such as O157:H7, can cause bloody diarrhea and abdominal cramps, and some people develop a type of kidney failure called hemolytic uremic syndrome (HUS).
- 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
- 127773 127829 127871 127936 127975 127986 128032 128036 128059 128133 128238 128247 128264 128291 128336 128383 128449 128482
- How many
- 10,482 cases
- Where it was sold
- Distribution Centers located in U.S. States: AL, AR, AZ, CA, CO, CT, FL, GA, HI, IA, ID, IL, IN, KS, KY, LA, MA, MD, MI, MN, MO, NC, NH, NJ, NM, NV, NY, OH, OK, OR, PA, RI, SC, TN, TX, UT, VA, VT, WA, WI U.S. Territories: Puerto Rico Foreign Countries: Canada, United Arab Emirates, Hong Kong, Columbia
- Status
- Terminated: FDA has closed the recall.
- Dates
- Recall started Nov 16, 2024; FDA classified it on Dec 31, 2024; reported in FDA's enforcement report on Jan 8, 2025.
- FDA recall number
- F-0357-2025
Grimmway Enterprises, Inc. dba Grimmway Farms · Jan 8, 2025
- Product
- --- Organic Baby Carrots --- Orangic Baby Peeled Carrots 13/3 BL; Orangic Baby Peeled Carrots 30/1 BL; Org Baby Peeled Carrots 12/2 Wholesome Pantry RPC; Org Baby Peeled Carrots 24/1 Wholesome Pantry RPC; Organic Baby Peeled Carrots 10/2/2Lb Cal O Display; Organic Baby Peeled Carrots 10/2/2Lb. Cal Organic; Organic Baby Peeled Carrots 12/1 Bunny Luv; Organic Baby Peeled Carrots 12/1 LIDL; Organic Baby Peeled Carrots 12/12oz Good & Gather; Organic Baby Peeled Carrots 12/2 Bunny Luv; Organic Baby Peeled Carrots 12/2 COF; Organic Baby Peeled Carrots 12/2 Pres Choice RPC; Organic Baby Peeled Carrots 13/3 BL; Organic Baby Peeled Carrots 15/2 365; Organic Baby Peeled Carrots 15/2 365 RPC; Organic Baby Peeled Carrots 15/2 BL; Organic Baby Peeled Carrots 15/2 COF; Organic Baby Peeled Carrots 15/2 Safeway O-Organic; Organic Baby Peeled Carrots 15/2 Sprouts; Organic Baby Peeled Carrots 18/2 Kroger RPC; Organic Baby Peeled Carrots 20/2 LB Marketside RPC; Organic Baby Peeled Carrots 20/2 Wegmans RPC; Organic Baby Peeled Carrots 24/1 BL; Organic Baby Peeled Carrots 24/1 Cal-Organic Farm; Organic Baby Peeled Carrots 24/1 Cal-Organic RPC; Organic Baby Peeled Carrots 24/1 Full Circle; Organic Baby Peeled Carrots 24/1 Good & Gather; Organic Baby Peeled Carrots 24/1 Greenwise; Organic Baby Peeled Carrots 24/1 Natures Promise; Organic Baby Peeled Carrots 24/1 Pres Choice RPC; Organic Baby Peeled Carrots 24/1 Simple Truth RPC; Organic Baby Peeled Carrots 24/12oz Wegman's; Organic Baby Peeled Carrots 30/1 365; Organic Baby Peeled Carrots 30/1 365 RPC; Organic Baby Peeled Carrots 30/1 BL; Organic Baby Peeled Carrots 30/1 Cal-Organic Farm; Organic Baby Peeled Carrots 30/1 Compliments; Organic Baby Peeled Carrots 30/1 Purely Made RPC; Organic Baby Peeled Carrots 30/1 Safeway O-Organic; Organic Baby Peeled Carrots 30/1 Sprouts; Organic Baby Peeled Carrots 30/1 TJ Petites 036679; Organic Baby Peeled Carrots 4/5 BL; Organic Baby Peeled Carrots 40/1 Marketside RPC; Organic Baby Peeled Carrots 40/1 Wegman's RPC; Organic Baby Peeled Petite Carrots 12/12oz 365; Organic Baby Pld Carrots 12/12oz O-Organic Petites --- Brands --- 365, Bunny Luv, Cal-Organic, Compliments, Full Circle, Good & Gather, GreenWise, LIDL, Marketside, Nature's Promise, O Organics, President's Choice, Purely Made, Simple Truth, Sprouts, Trader Joe's, Wegmans, Wholesome Pantry
- Why it was recalled
- Potential contamination with E. coli O121:H19 Some E. coli strains, such as O157:H7, can cause bloody diarrhea and abdominal cramps, and some people develop a type of kidney failure called hemolytic uremic syndrome (HUS).
- 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
- 127730 127734 127773 127777 127784 127829 127830 127834 127871 127875 127932 127936 127974 127975 127978 127986 128032 128036 128059 128063 128129 128133 128159 128163 128238 128246 128251 128264 128274 128286 128291 128336 128346 128347 128351 128365 128383 128449 128482 128550 127773 127829 128059 128159 128482
- How many
- 218,705 cases
- Where it was sold
- Distribution Centers located in U.S. States: AL, AR, AZ, CA, CO, CT, FL, GA, HI, IA, ID, IL, IN, KS, KY, LA, MA, MD, MI, MN, MO, NC, NH, NJ, NM, NV, NY, OH, OK, OR, PA, RI, SC, TN, TX, UT, VA, VT, WA, WI U.S. Territories: Puerto Rico Foreign Countries: Canada, United Arab Emirates, Hong Kong, Columbia
- Status
- Terminated: FDA has closed the recall.
- Dates
- Recall started Nov 16, 2024; FDA classified it on Dec 31, 2024; reported in FDA's enforcement report on Jan 8, 2025.
- FDA recall number
- F-0358-2025
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.