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 the agency’s own highest classification or reported deaths or serious injuries, 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 Cefoxitin in normal saline bags due to a lack of sterility assurance. The products were distributed in six states.
Walgreens Infusion Services is recalling ceftriaxone in normal saline due to a lack of sterility assurance. The products were distributed in six states.
Walgreens Infusion Services is recalling Thiamine 100 mg/ml vials 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 Acyclovir in normal saline due to lack of sterility assurance. The products were distributed in six states.
Mylan Institutional, Inc. is recalling Ciprofloxacin Tablets 500 mg because they were produced with active ingredients not manufactured according to Good Manufacturing Practices.
Walgreens Infusion Services is recalling Deferoxamine in normal saline due to a lack of sterility assurance. The products were distributed in six states.
Mylan Institutional is recalling 3,993 cartons of Lamotrigine 200 mg tablets because they were not manufactured according to Good Manufacturing Practices.
3M ESPE is recalling 19,728 tubes of Clinpro 5000 Anti-Cavity Toothpaste because the primary boxes are missing lot numbers and expiration dates.
SCA Pharmaceuticals is recalling 972 syringes of Glycopyrrolate injection distributed in Louisiana because a printing error made the expiration date appear incorrect.
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.
Actavis Elizabeth LLC is recalling specific lots of Gabapentin 400 mg capsules distributed in Puerto Rico due to clumping, breaking, and packaging defects.
Qualitest Pharmaceuticals is recalling specific lots of Acetaminophen and Codeine Phosphate Oral Solution because they failed impurity specifications for p-Aminophenol.
Aurobindo Pharma USA Inc is recalling 24,816 bottles of Gabapentin 300 mg capsules nationwide because of complaints that the capsules were empty.
Par Pharmaceutical is recalling one lot of HydrALAZINE Hydrochloride tablets because small aluminum particles were found in the product.
Actavis Elizabeth LLC is recalling GABA 300-EZS (Gabapentin) capsules distributed in Puerto Rico due to reports of clumping, breaking, and packaging defects.
Right Value Drug Stores is recalling specific lots of Glutathione 200 mg/mL Injectable because an incorrect gas was used to remove oxygen from the vials.
Actavis Elizabeth LLC is recalling 29,622 bottles of Gabapentin capsules distributed in Puerto Rico due to clumping, breaking, and packaging defects.
Akorn, Inc. is recalling 3,937 bottles of Triamcinolone Acetonide Lotion USP, 0.025% because a known impurity exceeded specifications at the 12-month stability point.
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.
One and Zen is recalling Ginseng Kianpi Pill capsules because FDA analysis found undeclared dexamethasone and cyproheptadine, making the product an unapproved drug.
Jaymac Pharmaceuticals is recalling J-TAN D PD Drops because the product is labeled 'Dye Free' but contains Red Dye 40.
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 12 vials of Glutathione 100mg/mL Sterile Injection 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.