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 Hydrochlorothiazide 12.5 mg tablets because they may be mislabeled as Chlordiazepoxide HCl 25 mg capsules.
Aidapak Services, LLC is recalling 1,001 tablets of 40 mg Pantoprazole Sodium due to a potential labeling mixup with Sennosides.
Aidapak Services is recalling Medroxyprogesterone Acetate tablets that may be mislabeled as Hydralazine HCl.
Aidapak Services, LLC is recalling Niacin TR tablets because they may be mislabeled as Solifenacin Succinate.
Aidapak Services, LLC is recalling 3 mg Melatonin tablets because they may be mislabeled as other medications like Docusate Sodium or Pioglitazone.
Greenstone LLC is recalling Nifedipine extended-release tablets because the package displays a 48-month expiration date instead of the correct 36-month date.
Aidapak Services, LLC is recalling Trazodone HCl 50 mg tablets because they may be mislabeled as Dexamethasone, Docusate Sodium, or Guanfacine.
Aidapak Services, LLC is recalling Zinc Glucosate tablets because they may be mislabeled as Ascorbic Acid chew tablets.
Aidapak Services is recalling Acetaminophen/Aspirin/Caffeine tablets that may be mislabeled as Naproxen. The error could lead to incorrect medication use.
Aidapak Services, LLC is recalling 1,821 tablets of Cyanocobalamin 1000 mcg due to a potential label mixup with other medications.
Aidapak Services is recalling Zinc Sulfate capsules that may be mislabeled as Calcium Acetate or Calcitrol due to a labeling mixup.
Aidapak Services, LLC is recalling Riluzole 50 mg tablets due to a labeling error where they may be mislabeled as Trazodone HCl 150 mg.
Aidapak Services, LLC is recalling Methylergonovine Maleate tablets because they may be mislabeled as Isosorbide Mononitrate or Levothyroxine Sodium.
Aidapak Services is recalling 10 mg Fosinopril Sodium tablets that may be mislabeled as Calcitriol capsules due to a labeling mixup.
Aidapak Services, LLC is recalling Vitamin B Complex Prolonged Release tablets because they may be mislabeled as other medications like Coenzyme Q-10 or Aspirin.
Aidapak Services, LLC is recalling Prenatal Multivitamin/Multimineral tablets because they may be mislabeled as Cyanocobalamin tablets. The error involves a label mixup.
Aidapak Services is recalling Magnesium Gluconate tablets that may be mislabeled as Fluvastatin capsules due to a label mixup.
Aidapak Services is recalling Promethazine HCL tablets that may be mislabeled as Cholecalciferol due to a labeling mixup.
Aidapak Services is recalling Flecaïnide Acetate tablets that may be mislabeled as Vitamin B Complex with C due to a labeling error.
Aidapak Services is recalling 1 mg melatonin tablets that may be mislabeled as cranberry extract or glycopyrrolate. The FDA classifies this as a Class II recall.
Aidapak Services is recalling Fluoxetine HCl capsules because they may be mislabeled as Pancrelipase DR.
Aidapak Services, LLC is recalling 799 Benazepril HCL tablets because they may be mislabeled as other medications.
Aidapak Services, LLC is recalling Atorvastatin Calcium 80 mg tablets because they may be mislabeled as Lactobacillus GG capsules.
Aidapak Services, LLC is recalling 500 mg Ascorbic Acid tablets that may be mislabeled as Febuxostat 40 mg. The error could lead to incorrect medication administration.
Aidapak Services is recalling 1,300 Quetiapine Fumarate 100 mg tablets because they may be mislabeled as other medications.