Recalls — last 90 days
- 2026-05-27FDA-FoodLIQUID BLENZ CORPClass IIFlat Belly Bully drink recalled for botulism risk
May be under-processed resulting in growth of Clostridium botulinum and lists health claims.
- 2026-05-27FDA-FoodLIQUID BLENZ CORPClass IILiquid Blenz Blood Pressure Bully recalled for botulism risk
May be under-processed resulting in growth of Clostridium botulinum and lists health claims.
- 2026-05-27FDA-FoodLIQUID BLENZ CORPClass IILiquid Blenz Pure Shilajit Tonic recalled for botulism risk
May be under-processed resulting in growth of Clostridium botulinum and lists health claims.
- 2026-05-27FDA-FoodLIQUID BLENZ CORPClass IILiquid Blenz Prostate Bully recalled for botulism risk
May be under-processed resulting in growth of Clostridium botulinum and lists health claims.
- 2026-05-27FDA-FoodLIQUID BLENZ CORPClass IILiquid Blenz Fibroid Bully recalled for botulism risk
May be under-processed resulting in growth of Clostridium botulinum and lists health claims.
- 2026-05-27FDA-FoodLIQUID BLENZ CORPClass IILiquid Blenz Menopause Bully recalled for botulism risk
May be under-processed resulting in growth of Clostridium botulinum and lists health claims.
- 2026-05-27FDA-FoodLIQUID BLENZ CORPClass IILiquid Blenz Elderberry syrup recalled for botulism risk
May be under-processed resulting in growth of Clostridium botulinum and lists health claims.
- 2026-05-27FDA-FoodLIQUID BLENZ CORPClass IIPure Libido Drink recalled for botulism risk
May be under-processed resulting in growth of Clostridium botulinum and lists health claims.
- 2026-05-27FDA-FoodLIQUID BLENZ CORPClass IILiquid Blenz Pure Diabetes Bully recalled for botulism risk
May be under-processed resulting in growth of Clostridium botulinum and lists health claims.
- 2026-05-27FDA-FoodLIQUID BLENZ CORPClass IILiquid Blenz Sea Moss Tonic recalled for botulism risk
May be under-processed resulting in growth of Clostridium botulinum and lists health claims.
- 2026-05-27FDA-FoodLIQUID BLENZ CORPClass IILiquid Blenz Blackseed Bitters recalled for botulism risk
May be under-processed resulting in growth of Clostridium botulinum and lists health claims.
- 2026-05-27FDA-FoodLIQUID BLENZ CORPClass IILiquid Blenz Soursop Bitters recalled for botulism risk
May be under-processed resulting in growth of Clostridium botulinum and lists health claims.
- 2026-05-27FDA-DrugWisconsin Pharmacal CompanyClass IMG217 skin cream recalled for bacterial contamination
Microbial Contamination of Non-Sterile Products: confirmed presence of Staphylococcus Aureus.
- 2026-05-27FDA-DrugSafecor Health, LLCClass IISafecor Health Nephronex vitamin supplement recalled for foreign particles
Presence of a Foreign Substance; black particles observed in liquid
- 2026-05-27FDA-DrugIntegraDose Compounding Services LLCClass IIIntegraDose fentanyl citrate injection recalled for subpotency
Subpotent Drug
- 2026-05-27FDA-DrugUCB Biosciences Inc.Class IICimzia prefilled syringes recalled for sterility concerns
Lack of Assurance of Sterility
- 2026-05-27FDA-DrugZydus Pharmaceuticals (USA) IncClass IIZydus erythromycin tablets recalled for nitrosamine impurity
CGMP Deviations; presence of N-Nitroso-Desmethyl-Erythromycin above the recommended acceptable intake limit
- 2026-05-27FDA-DrugZydus Pharmaceuticals (USA) IncClass IIZydus erythromycin tablets recalled for nitrosamine impurity
CGMP Deviations; presence of N-Nitroso-Desmethyl-Erythromycin above the recommended acceptable intake limit
- 2026-05-27FDA-DrugANI Pharmaceuticals, Inc.Class IIANI Pharmaceuticals estradiol gel recalled for defective packets
Defective Container; packets were found to be either empty or partially full.
- 2026-05-27FDA-DrugHaleon US Holdings LLCClass IIGas-X Simethicone recalled for incomplete ingredient labeling
Labeling: Not Elsewhere Classified- Incomplete inactive ingredient information on the carton labeling.
- 2026-05-27FDA-DrugLupin Pharmaceuticals Inc.Class IILupin Liraglutide Injection recalled for particulate matter
Presence of particulate matter: a white thread-like structure in the cartridge
- 2026-05-27FDA-DrugSagent PharmaceuticalsClass IIISagent Busulfan Injection recalled for impurity specifications failure
Failed Impurities/Degradation Specifications
- 2026-05-27FDA-DrugSafecor Health, LLCClass IISafecor Health atomoxetine capsules mislabeled with wrong strength
Labeling: Label Mix-Up: Atomoxetine HCl 25mg Capsule incorrectly labeled as Atomoxetine HCl 10mg Capsule.
- 2026-05-27FDA-DrugAmerisource Health Services LLCClass IIIAmerisource Primidone Tablets recalled for contamination
Cross contamination with other products: API contaminated with trace amounts of Acemetacin API.
- 2026-05-27FDA-DrugAmerisource Health Services LLCClass IIIAmerisource Primidone tablets recalled for cross-contamination
Cross contamination with other products: API contaminated with trace amounts of Acemetacin API.
- 2026-05-27FDA-DrugGolden State Medical Supply Inc.Class IIIGolden State Medical Supply Primidone Tablets recalled for contamination
Cross contamination with other products: API contaminated with trace amounts of Acemetacin API.
- 2026-05-27FDA-DrugGolden State Medical Supply Inc.Class IIIGolden State Medical Supply Primidone recalled for API contamination
Cross contamination with other products: API contaminated with trace amounts of Acemetacin API.
- 2026-05-27FDA-DrugLannett Company Inc.Class IIILannett Primidone tablets recalled for API contamination
Cross contamination with other products: API contaminated with trace amounts of Acemetacin API.
- 2026-05-26FDA-PRTotal Nutrition Inc.TNVitamins and Doctor's Pride moringa capsules recalled for Salmonella
Total Nutrition Inc. of Deer Park, NY is voluntarily recalling TNVitamins Ultra Potent Complete Green Superfood and Doctor’s Pride Complete Green Superfood Ultra Potent Moringa Capsules (120 count) because they have the potential to be contaminated with Salmonella, an organism which can cause seriou
- 2026-05-26FDA-PROmnipod insulin pods recalled for under-delivery risk
ACTON, Mass.--(BUSINESS WIRE)-- Insulet Corporation, Inc. (NASDAQ: PODD) (“Insulet” or the “Company”) today announced a voluntary Medical Device Correction for specific lots of Omnipod® 5, Omnipod DASH®, and Omnipod® Insulin Management System (Omnipod Eros) Pods due to a manufacturing issue, identif