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
Aidapak Services, LLC is recalling Nebivolol HCL 5 mg tablets because they may have been mislabeled as Thyroid or Rasagiline Mesylate.
Aidapak Services, LLC is recalling Levothyroxine Sodium tablets that may have been mislabeled as Omega-3 Fatty Acid capsules.
Aidapak Services, LLC is recalling Sotalol HCL 160 mg tablets that may have been mislabeled as Disulfiram 250 mg.
Aidapak Services, LLC is recalling Phenobarbital 97.2 mg tablets because they may have been mislabeled as 64.8 mg tablets.
Aidapak Services, LLC is recalling Bumetanide 0.5 mg tablets because they may have been mislabeled as Erythromycin DR EC 250 mg.
Aidapak Services, LLC is recalling Nortriptyline HCL capsules because they may have been mislabeled as Rosuvastatin Calcium or Liothyronine Sodium.
Aidapak Services, LLC is recalling Trihexyphenidyl HCL tablets because they may have been mislabeled as Perphenazine tablets.
Aidapak Services, LLC is recalling Nifedipine ER 60 mg tablets because they may have been mislabeled as Nicotine Polacrilex 2 mg lozenges.
Aidapak Services is recalling Pancrelipase DR capsules due to a potential label mixup with Aspirin/ER Dipyridamole. The repacked drugs were distributed in four western states.
Aidapak Services, LLC is recalling azaTHIOprine 50 mg tablets because they may have been mislabeled as Selenium 50 mcg tablets.
Aidapak Services, LLC is recalling Isoniazid 300 mg tablets because they may have been mislabeled as other prescription drugs.
Aidapak Services, LLC is recalling Sennosides tablets because they may have been mislabeled as other medications. The recall covers distribution in four western states.
Aidapak Services, LLC is recalling Nefazodone HCL 200 mg tablets because they may have been mislabeled as 150 mg tablets.
Novartis is recalling NeoCitran and Theraflu cold and sinus powder packets because they may contain foreign substances.
Aidapak Services, LLC is recalling Multivitamin/Multimineral Chew Tablets due to a potential label mixup with Cholecalciferol capsules. The mislabeled products were distributed in four western states.
Aidapak Services is recalling Levothyroxine Sodium tablets because they may have been mislabeled as other prescription drugs.
Aidapak Services, LLC is recalling CapsuleTOPRIL 25 mg tablets because they may have been mislabeled as Duloxetine HCl DR 20 mg capsules.
Aidapak Services, LLC is recalling Lithium Carbonate ER tablets because they may be mislabeled as Vitamin B Complex Prolonged Release tablets.
Aidapak Services, LLC is recalling Imipramine HCL 25 mg tablets because they may have been mislabeled as Fenofibrate 54 mg.
Novartis Consumer Health is recalling Theraflu Exte powder packets because they may contain foreign substances. The recall covers products distributed in the U.S. and several international markets.
Aidapak Services, LLC is recalling 500 mg Mycophenolate Mofetil tablets because they may be mislabeled as 250 mg capsules.
Aidapak Services is recalling Mycophenolate Mofetil capsules due to a potential label mixup with Calcium Acetate.
Aidapak Services, LLC is recalling 60 mg Thyroid tablets that may have been mislabeled as 30 mg tablets.
Aidapak Services, LLC is recalling Albuterol Sulfate ER 4 mg tablets that may have been mislabeled as Simvastatin 20 mg.
Aidapak Services, LLC is recalling Levothyroxine Sodium tablets due to a potential label mixup with Magnesium Chloride. The repacked drugs were distributed in four western states.