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
Amneal Pharmaceuticals is recalling Nizatidine Oral Solution because it may contain N-Nitrosodimethylamine (NDMA) levels above FDA limits.
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.
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.
Lupin Pharmaceuticals is recalling 20 mg Lisinopril tablets because 10 mg tablets were found inside sealed 20 mg bottles.
Yusef Manufacturing is recalling 12,983 tubes of SPF 15 lip moisturizers because they contain up to 150% of the labeled amount of oxybenzone.
Noven Therapeutics is recalling Daytrana (methylphenidate) transdermal patches because the delivery system failed mechanical peel and shear specifications.
Noven Therapeutics is recalling Daytrana (methylphenidate) transdermal systems because the delivery system failed mechanical peel and shear specifications.
Lupin Pharmaceuticals is recalling 4,518 bottles of Cefixime for Oral Suspension because a stability study showed the drug was below the required strength.
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 Levothyroxin/Liothyronine SR capsules due to a lack of processing control. The affected 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.
The Medicine Shoppe Pharmacy is recalling Bi-Est cream due to lack of processing control. The product was distributed in Florida.
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 specific lots of Testosterone in Atrevis 75 mg/mL Gel due to a lack of processing control. The affected product was distributed in Florida.
The FDA is recalling Bi-Est/DHEA/Testosterone cream from The Medicine Shoppe Pharmacy in Florida due to a lack of processing control.
Aurobindo Pharma USA Inc. is recalling specific lots of Acetaminophen and Codeine Phosphate tablets because they were manufactured in an area with observed water leakage.
The Medicine Shoppe Pharmacy in Port Charlotte, Florida, is recalling Hydroquinone/Fluocinolone/Tretonoin/Kojic Acid cream due to a lack of processing control.
The Medicine Shoppe Pharmacy is recalling Ergotamine Tartrate and Caffeine suppositories due to a lack of processing control.
Aurobindo Pharma is recalling 8,040 bottles of Levetiracetam 750 mg tablets because they were manufactured in an area with observed water leakage.
The Medicine Shoppe Pharmacy is recalling Betahistine 16 mg capsules due to lack of processing control. The recall affects 2 bottles distributed in Florida.
The Medicine Shoppe Pharmacy is recalling Bi-Est cream due to a lack of processing control. The product was distributed in Florida.
The Medicine Shoppe Pharmacy is recalling Bi-Est Cream due to a lack of processing control. The product was distributed in Florida.
The Medicine Shoppe Pharmacy in Port Charlotte, Florida, is recalling Bi-Est8:2/Progesterone/Testosterone cream due to a lack of processing control. The recall affects one tube of the product.
The Medicine Shoppe Pharmacy is recalling Bi-Est Cream due to lack of processing control. The product was distributed in Florida.