FDA Recall
🇺🇸 United States
TerminatedTerminated: March 26, 2025Historical recordClass II
ZB Importing LLC
- Product
- Ulker Kekstra Mini strawberry, item 3792, 5.3oz foil pack, 1…
- Reason
- Milk not declared as the major food allergen source for the ingredient Whey
- Published
- March 19, 2025
- Distribution
- Products were distributed through retail…
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FDA Recall
🇺🇸 United States
OngoingHistorical recordClass II
DANONE WAVE
- Product
- HAZELNUT INTERNATIONAL delight COFFEE CREAMER 32 FL OZ (1 QT…
- Reason
- The firm received complaints of spoilage and illness with the use of the products.
- Published
- March 19, 2025
- Distribution
- The product was shipped to the following…
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FDA Recall
🇺🇸 United States
TerminatedTerminated: August 12, 2025Historical recordClass II
Shearer's Foods, LLC
- Product
- 1.) Market Pantry Soup & Oyster Crackers, NET WT 9 OZ (255g)…
- Reason
- Potential foreign material (stainless steel wire)
- Published
- March 19, 2025
- Distribution
- Product distributed to customers in the…
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FDA Recall
🇺🇸 United States
OngoingHistorical recordClass II
Chicken of the Sea; Thai Union
- Product
- HEB branded Solid White Albacore Tuna in water; Wild Caught;…
- Reason
- Product's easy-pull lid was not secured properly and may cause the product to become adulterated with the hazard clostridium botulinum.
- Published
- March 19, 2025
- Distribution
- Nationwide
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FDA Recall
🇺🇸 United States
OngoingHistorical recordClass II
Chicken of the Sea; Thai Union
- Product
- Trader Joe's branded Solid White Albacore Tuna in Water, no…
- Reason
- Product's easy-pull lid was not secured properly and may cause the product to become adulterated with the hazard clostridium botulinum.
- Published
- March 19, 2025
- Distribution
- Nationwide
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FDA Recall
🇺🇸 United States
OngoingHistorical recordClass II
Chicken of the Sea; Thai Union
- Product
- Genova branded Solid white Tuna; In Olive Oil; Wild Caught;…
- Reason
- Product's easy-pull lid was not secured properly and may cause the product to become adulterated with the hazard clostridium botulinum.
- Published
- March 19, 2025
- Distribution
- Nationwide
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FDA Recall
OngoingHistorical recordClass II
Nelarabine Injection, 250mg/50mL, (5mg/mL), packaged in: a) 50 mL Single-Dose Vial, NDC 70710-1839-1; b) 6 x 50 mL Single-Dose Vial, NDC 70710-1839-8, Rx only, Manufactured by Zydus Lifesciences Ltd, Ahmedabad, India, Distributed by: Zydus Pharmaceuticals (USA) Inc, Pennington, NJ
by Zydus Pharmaceuticals (USA) Inc
- Reason
- Failed Impurities/Degradation Specifications
- Published
- March 12, 2025
- Distribution
- Nationwide
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FDA Recall
OngoingHistorical recordClass II
Nelarabine Injection, 250mg/50mL, (5mg/mL), packaged in: a) 50 mL Single-Dose Vial, NDC 70710-1726-1; b) 6 x 50 mL Single-Dose Vial, NDC 70710-1726-8, Rx only, Manufactured by Zydus Lifesciences Ltd, Ahmedabad, India, Distributed by: Zydus Pharmaceuticals (USA) Inc, Pennington, NJ
by Zydus Pharmaceuticals (USA) Inc
- Reason
- Failed Impurities/Degradation Specifications
- Published
- March 12, 2025
- Distribution
- Nationwide
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FDA Recall
OngoingHistorical recordClass II
Morphine Sulfate 5 mg per 0.25 mL Oral Syringe, Delivers: 0.25 mL, Oral Solution, Rx Only, Mfg by: Hikma, Pkg by: Safecor Health, LLC, Columbus, OH 43204, NDC: a) 00406800312, b) 00406800330, c) 00054051750.
by Safecor Health, LLC
- Reason
- Defective Delivery System: Leakage observed after oral solution was repackaged into unit-dose syringes.
- Published
- March 12, 2025
- Distribution
- Nationwide
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FDA Recall
OngoingHistorical recordClass II
Lorazepam 0.5 mg per 0.25 mL Oral Syringe, Delivers: 0.25 mL, Oral Concentrate, Rx Only, Refrigerate, Mfg by: PAI, Pkg by: Safecor Health, LLC, Columbus, OH 43204, NDC: a) 00054353244, b) 00121077001, c) 65162068784.
by Safecor Health, LLC
- Reason
- Defective Delivery System: Leakage observed after oral solution was repackaged into unit-dose syringes.
- Published
- March 12, 2025
- Distribution
- Nationwide
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FDA Recall
OngoingHistorical recordClass II
Ferrous Sulfate 7.5 mg Iron/0.5 mL Oral Syringe, Delivers: 0.5 mL, Iron Supplement Drops, Mfg by: Akron Pharma, Pkg by: Safecor, Columbus, OH 43204. NDC: a) 71399748005, b) 39328055750, c) 69618007059.
by Safecor Health, LLC
- Reason
- Defective Delivery System: Leakage observed after oral solution was repackaged into unit-dose syringes.
- Published
- March 12, 2025
- Distribution
- Nationwide
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FDA Recall
OngoingHistorical recordClass II
Simethicone 20 mg per 0.3 mL Oral Syringe, Delivers: 0.3 mL, Oral Drops, Mfg By: Rugby, Pkg by: Safecor Health, LLC, Columbus, OH 43204, NDC: 00536130375.
by Safecor Health, LLC
- Reason
- Defective Delivery System: Leakage observed after oral solution was repackaged into unit-dose syringes.
- Published
- March 12, 2025
- Distribution
- Nationwide
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FDA Recall
OngoingHistorical recordClass II
Ergocalciferol - Vitamin D Supplement - 10 mcg (400 Units) per 0.05 mL Oral Syringe, Delivers: 0.05 mL Oral Solution, Mfg by: Westminster, Pkg by: Safecor Health, LLC, Columbus, OH 43204, NDC: 69367028302.
by Safecor Health, LLC
- Reason
- Defective Delivery System: Leakage observed after oral solution was repackaged into unit-dose syringes.
- Published
- March 12, 2025
- Distribution
- Nationwide
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FDA Recall
OngoingHistorical recordClass II
Morphine Sulfate Extended-Release Tablets, 100 mg, 100-count bottles, Rx Only, Manufactured by: Ohm Laboratories Inc., New Brunswick, NJ 08901. Distributed by: Sun Pharmaceutical Industries, Inc., Cranbury, NJ 08512. NDC 63304-452-01
by SUN PHARMACEUTICAL INDUSTRIES INC
- Reason
- Failed Dissolution Specifications
- Published
- March 12, 2025
- Distribution
- Nationwide
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FDA Recall
🇺🇸 United States
TerminatedTerminated: April 8, 2025Historical recordClass I
Amazon Retail LLC
- Product
- ASIN B0CY2RDW5T, Amazon Fresh brand, Bake at Home Jumbo Suga…
- Reason
- Undeclared egg.
- Published
- March 12, 2025
- Distribution
- Nationwide
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FDA Recall
🇺🇸 United States
TerminatedTerminated: April 8, 2025Historical recordClass I
Amazon Retail LLC
- Product
- ASIN B084PZ7K98, Amazon Fresh Jumbo Sugar Cookie, 27 oz (12…
- Reason
- Undeclared egg.
- Published
- March 12, 2025
- Distribution
- Nationwide
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FDA Recall
CompletedTerminated: February 26, 2026Historical recordClass II
Avastin 1.25 mg/0.05 mL in 0.25 mL Syringe, For Intravitreal Injection Only, Office Use Only - Not for Resale - Single Use, This drug product was repackaged by Turbare Manufacturing, 925 Jeanette Drive, Conway, AR 72032, NDC: 83556-0101-01.
by Turbare Manufacturing
- Reason
- Lack of Assurance of Sterility: due to a quality control process deviation
- Published
- March 5, 2025
- Distribution
- Nationwide
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FDA Recall
CompletedHistorical recordClass II
Estradiol Gel, 0.1%, 0.25 mg/g, 30 packets per carton, Rx Only, For Topical Use Only, Manufactured by Padagis, Yeruham, Israel, NDC: 45802-0134-30
by Padagis US LLC
- Reason
- Defective Container: Some packets may not be fully sealed, potentially allowing for loss of Ethanol from the product.
- Published
- March 5, 2025
- Distribution
- Nationwide
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FDA Recall
🇺🇸 United States
TerminatedTerminated: March 21, 2025Historical recordClass II
V Chocolates, Inc
- Product
- Assorted Chocolate Caramels with kosher sea salt, Net Weight…
- Reason
- Small pieces of plastic broken tray in the product.
- Published
- March 5, 2025
- Distribution
- Nationwide
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FDA Recall
🇺🇸 United States
TerminatedTerminated: July 22, 2025Historical recordClass I
Nestle-USA, Inc. (Corporate Office)
- Product
- Gerber Snacks for Baby Soothe 'n' Chew TEETHING STICKS Banan…
- Reason
- Firm received complaints of infant choking.
- Published
- March 5, 2025
- Distribution
- The products were shipped to distributio…
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Recall records are summarized from official FDA and USDA sources. Notices may be updated, reclassified, terminated, or withdrawn. Always review the linked official notice for the most current instructions.
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