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
The Harvard Drug Group is recalling 678 cartons of Memantine Hydrochloride Extended-Release Capsules due to low stage 3 dissolution results found during routine stability testing.
Glaxosmithkline is recalling 288 packages of ChapStick Total Hydration Moisture Tint Peachy Keen due to observed separation in the secondary packaging.
Glaxosmithkline is recalling ChapStick Total Hydration Moisture Tint Pretty in Pink due to observed separation in the secondary packaging.
Glaxosmithkline is recalling ChapStick Total Hydration Moisture Tint Very Berry due to observed separation in the secondary packaging.
Sandoz is recalling 17,500 units of Infuvite Pediatric Multiple Vitamins Injection due to sub-optimal crimping in the vial. The product was distributed nationwide.
Teva Pharmaceuticals is recalling Epinephrine Injection USP auto-injectors due to out-of-specification trigger force. The product was not distributed to the public.
B. Braun Medical Inc. is recalling one lot of Ceftazidime for Injection USP and Dextrose for Injection USP because the product failed stability specifications for high molecular weight polymers.
Amneal Pharmaceuticals is recalling Nizatidine Oral Solution because it may contain N-Nitrosodimethylamine (NDMA) levels above FDA limits.
Dr. Reddy's Laboratories is recalling 1,752 bottles of Esomeprazole Magnesium 40 mg capsules because the product contains brown pellets.
Noven Therapeutics is recalling Daytrana (methylphenidate) transdermal patches because the delivery system failed mechanical peel and shear specifications.
Yusef Manufacturing is recalling 12,983 tubes of SPF 15 lip moisturizers because they contain up to 150% of the labeled amount of oxybenzone.
Lupin Pharmaceuticals is recalling 20 mg Lisinopril tablets because 10 mg tablets were found inside sealed 20 mg bottles.
Lupin Pharmaceuticals is recalling 4,518 bottles of Cefixime for Oral Suspension because a stability study showed the drug was below the required strength.
Noven Therapeutics is recalling Daytrana (methylphenidate) transdermal systems because the delivery system failed mechanical peel and shear specifications.
Noven Therapeutics is recalling Daytrana (methylphenidate) transdermal patches because the delivery system failed mechanical peel and shear specifications.
The Medicine Shoppe Pharmacy is recalling Levothyroxin/Liothyronine SR capsules due to a lack of processing control. The affected product was distributed in Florida.
The Medicine Shoppe Pharmacy is recalling Bi-Est cream due to lack of processing control. The product was distributed in Florida.
Golden State Medical Supply Inc. is recalling Losartan Potassium Tablets 25 mg because an impurity, NBMA, was detected in the active ingredient.
Aurobindo Pharma USA Inc. is recalling specific lots of Gabapentin Capsules because they were manufactured in an area with observed water leakage.
The Medicine Shoppe Pharmacy is recalling Ergotamine Tartrate and Caffeine suppositories in Florida due to a lack of processing control.
Aurobindo Pharma USA Inc. is recalling 2,101 bottles of Phentermine Hydrochloride 15mg capsules because they were manufactured in an area with observed water leakage.
The Medicine Shoppe Pharmacy is recalling Estriol 5 mg Suppositories due to a lack of processing control. The affected lot is distributed in Florida.
The Medicine Shoppe Pharmacy is recalling Bi-Est Cream due to lack of processing control. The product was distributed in Florida.
The Medicine Shoppe Pharmacy is recalling Bi-Est 1:1/Progest/DHEA 1/40/5 mg/mL Cream due to lack of processing control.
The Medicine Shoppe Pharmacy in Port Charlotte, Florida, is recalling Hydroquinone/Fluocinolone/Tretonoin/Kojic Acid cream due to a lack of processing control.