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
Abbott's Compounding Pharmacy is recalling all unexpired lots of sterile compounded products after FDA inspection found concerns regarding lack of sterility assurance.
Abbott's Compounding Pharmacy is recalling all unexpired lots of sterile compounded products after an FDA inspection identified concerns regarding the lack of sterility assurance.
Abbott's Compounding Pharmacy is recalling all unexpired lots of compounded testosterone cypionate after an FDA inspection identified concerns regarding the assurance of sterility.
Abbott's Compounding Pharmacy is recalling all unexpired lots of papaverine phent sterile compounded products because an FDA inspection found concerns regarding the assurance of sterility.
Abbott's Compounding Pharmacy is recalling all unexpired lots of sterile compounded products after FDA inspection identified concerns regarding lack of sterility assurance.
Abbott's Compounding Pharmacy is recalling all unexpired lots of sterile compounded products after FDA inspection found concerns regarding lack of sterility assurance.
Abbott's Compounding Pharmacy is recalling all unexpired lots of Bupivacaine 0.25% sterile compounded products because an FDA inspection found concerns regarding the lack of sterility assurance.
Abbott's Compounding Pharmacy is recalling all unexpired lots of sterile compounded products, including papaverine phentolamine prostaglandin, after FDA inspection found concerns regarding lack of sterility assurance.
Abbott's Compounding Pharmacy is recalling all unexpired lots of sterile compounded products, including papaverine phentolamine, after FDA inspection found concerns regarding lack of sterility assurance.
Abbott's Compounding Pharmacy is recalling all unexpired lots of methylcobalamine 4 mg/mL in California due to FDA findings of lack of sterility assurance.
Abbott's Compounding Pharmacy is recalling all unexpired lots of sterile compounded products, including papaverine phentolamine prostaglandin, after FDA inspection found lack of sterility assurance.
Abbott's Compounding Pharmacy is recalling all unexpired lots of sterile methylcobalamine injections because an FDA inspection found concerns regarding the assurance of sterility.
Abbott's Compounding Pharmacy is recalling all unexpired lots of sterile compounded products, including progesterone/testosterone, due to lack of sterility assurance found during an FDA inspection.
Abbott's Compounding Pharmacy is recalling all unexpired lots of sterile compounded products, including papaverine prostaglandin, after FDA inspection found lack of sterility assurance.
Bonita Pharmaceuticals is recalling Menthocin Patch with Lidocaine-Strong because it was marketed without an approved NDA or ANDA.
Dr. Reddy's Laboratories is recalling 11,123 bottles of Paricalcitol capsules nationwide because the capsules have broken and leaked.
Dr. Reddy's Laboratories is recalling Paricalcitol capsules due to reports of breakage and leakage. The recall covers 4,383 bottles distributed nationwide.
Dr. Reddy's Laboratories is recalling 9,155 bottles of Paricalcitol capsules nationwide due to reports of breakage and leakage.
Pharmedium Services, LLC is recalling 19 syringes of Morphine Sulfate in Wisconsin because the drug was found to be subpotent.
Macleods Pharma USA is recalling Pramipexole Dihydrochloride tablets due to the presence of a foreign Carbimazole 5 mg tablet.
Fagron, Inc. is recalling SyrSpend SF Grape Flavor suspending base due to the presence of yeast. The recall affects 148 bottles distributed nationwide.
Safecor Health is recalling 3,532 bottles of Haloperidol Oral Solution because customer complaints confirmed the bottles were leaking.
Fagron, Inc. is recalling SyrSpend SF Suspending Base because the product contains yeast. The recall covers 88 bottles distributed nationwide.
Sandoz Inc. is recalling Candesartan Cilexetil Tablets, 16 mg, because the product failed impurities and degradation specifications at a 9-month stability timepoint.
Safecor Health is recalling specific lots of Midazolam HCl Syrup unit dose cups found to contain a small piece of cardboard.