Recalls
Searchable archive of product recalls from the FDA, USDA FSIS, CPSC, NHTSA, and EPA — translated into plain English, severity-scored from objective criteria, and always linked back to the original government notice.
Every recall on this list has been scored 1–5 against an objective rubric from the agency’s own classification, presence of reported injuries or deaths, distribution scope, and hazard type. The colored severity badge on each card is the score — 5 (Critical) means deaths or serious injuries are reported, 4 (Severe) means significant injury or hospitalization risk, and 3 (High) means a known hazard with no confirmed harm yet. Filter to 3+ (High and above) if you want to skip routine Class-III notices.
The agency chips above control which streams are visible. FDA spans food, drugs, and medical devices. USDA FSIS is meat, poultry, and processed egg products. CPSC is household consumer products. NHTSA is vehicles, tires, and child seats. Nationwide on a card means the recall affects every US state — most do — while a state list means distribution was limited.
Click any recall to see the full summary, affected lot codes and model numbers, the agency’s own classification, and a direct link back to the original government notice for verification.
Minimum severity
Walgreens Infusion Services is recalling Caspofungin in normal saline due to a lack of sterility assurance. The products were distributed in six states.
Walgreens Infusion Services is recalling Amikacin in normal saline bags due to a lack of sterility assurance. The products were distributed in six states.
Walgreens Infusion Services is recalling Dopamine in dextrose due to a lack of sterility assurance. The products were distributed in six states.
Walgreens Infusion Services is recalling Tigecycline in normal saline due to a lack of sterility assurance. The products were distributed in six southern states.
Walgreens Infusion Services is recalling Vancomycin in normal saline bags due to a lack of sterility assurance. The products were distributed in six states.
Walgreens Infusion Services is recalling Nafcillin injection bags in several states due to a lack of sterility assurance.
Walgreens Infusion Services is recalling L-cysteine products due to a lack of sterility assurance. The affected products were distributed in six southern states.
Walgreens Infusion Services is recalling Acyclovir in normal saline due to lack of sterility assurance. The products were distributed in six states.
Hospira Inc. is recalling 30,840 bags of 0.9% Sodium Chloride Injection, USP, 100mL, due to a potential leak at the administrative port that compromises sterility.
One and Zen is recalling Ginseng Kianpi Pill capsules because FDA analysis found undeclared dexamethasone and cyproheptadine, making the product an unapproved drug.
Tropichem Research Labs is recalling Entertainer's Secret Throat Relief due to microbial contamination, including E. Coli. The product was distributed in New York and Indiana.
Pharmacy Creations is recalling 52 vials of Magnesium Chloride 20% Injection because contract testing indicated the product may not be sterile.
Pharmacy Creations is recalling 50 bottles of Tropi/Cyclo/Phenyl/Tobra/Flurb sterile ophthalmic solution due to failing sterility test results.
Pharmacy Creations is recalling 67 vials of Ascorbic Acid 500 mg/mL Sterile Injection because contract testing indicated the product may not be sterile.
Pharmacy Creations is recalling 12 vials of Glutathione 100mg/mL Sterile Injection due to failing sterility test results.
Vann Healthcare Services is recalling Lidocaine 4% syringes because an FDA inspection found deficiencies in the facility's ability to assure sterility.
New Life Nutritional Center is recalling specific weight loss and dietary supplement products because they contain undeclared and unapproved drugs.
New Life Nutritional Center is recalling Esmeralda, Super Fat Burner, and Maxi Gold Weight Loss Pill due to undeclared and unapproved drugs.
Hospira is recalling 63,378 units of Heparin Sodium injection because human hair was found sealed inside the container's administration port.
Chaotic Labz is recalling MAYHEM capsules because FDA analysis found undeclared dexamethasone and cyproheptadine, making the product an unapproved drug.
Vann Healthcare Services is recalling 410 epinephrine syringes because an FDA inspection found deficiencies that raise concerns about the pharmacy's ability to assure sterility.
Vann Healthcare Pharmacy is recalling Tri-mix #4 vials because an FDA inspection found deficiencies that raise concerns about the pharmacy's ability to consistently assure sterility.
New Life Nutritional Center is recalling Super Fat Burner and other products because they contain undeclared and unapproved drugs.
Hospira Inc. is recalling Meropenem I.V. 1 g vials because thin glass walls may crack, leading to contamination and sterility issues.
Fresenius Kabi USA is recalling 101,200 vials of Midazolam Hydrochloride Injection due to potential glass fractures and particles that compromise sterility.