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 is recalling ferrous sulfate tablets that may be mislabeled as ramipril capsules. The error involves a label mixup on repacked drugs.
Aidapak Services, LLC is recalling 1 mg Folic Acid tablets because they may be mislabeled as other medications. The repacked drugs were distributed in four western states.
Aidapak Services, LLC is recalling Glucosamine/Chondroitin capsules because they may be mislabeled as Fexofenadine HCL tablets.
Aidapak Services is recalling Multivitamin/Multimineral Chew Tablets because they may be mislabeled as Levothyroxine Sodium or Lactobacillus Acidophilus.
Aidapak Services, LLC is recalling OXcarbazepine 600 mg tablets that may be mislabeled as Lactase Enzyme 3000 units. The error could lead to patients receiving the wrong medication.
Aidapak Services is recalling Zinc Sulfate capsules that may be mislabeled as Sertraline HCL tablets. The error could lead to patients taking the wrong medication.
Aidapak Services is recalling Cilostazol 100 mg tablets due to a labeling mixup where they may be mislabeled as Dutasteride 0.5 mg capsules.
Aidapak Services, LLC is recalling 150 mg Irbesartan tablets because they may be mislabeled as Atropine Sulfate/Diphenoxylate HCl or Cholecalciferol.
Aidapak Services is recalling Magnesium Gluconate Dihydrate tablets because they may be mislabeled as hydrALAZINE HCl.
Aidapak Services, LLC is recalling Cyproheptadine HCL 4 mg tablets because they may be mislabeled as other medications.
Aidapak Services is recalling Nifedipine 10 mg capsules due to a potential label mixup with multivitamin products.
Aidapak Services, LLC is recalling Zinc Sulfate capsules that may be mislabeled as Phosphorus tablets. The error involves a label mixup on repacked products.
Aidapak Services, LLC is recalling Lactobacillus GG capsules because they may be mislabeled as guaiFENesin ER tablets. The repacked drugs were distributed in four western states.
Aidapak Services, LLC is recalling Tizanidine HCL tablets because they may be mislabeled as Nicotine Polacrilex or Nifedipine ER.
Aidapak Services, LLC is recalling Esterified Estrogens tablets because they may be mislabeled as Etodolac. The repacked drugs were distributed in four western states.
Aidapak Services is recalling 1000 mg Omega-3 Fatty Acid capsules because they may be mislabeled as Nortriptyline HCL 50 mg.
Aidapak Services, LLC is recalling Vitamin B Complex tablets because they may be mislabeled as Omeprazole or Prednisone.
Aidapak Services is recalling Erythromycin DR EC tablets that may be mislabeled as methylprednisolone. The error could lead to patients receiving the wrong medication.
Aidapak Services, LLC is recalling 5,000-unit Cholecalciferol capsules because they may be mislabeled as other medications. The repacked drugs were distributed in four western states.
Aidapak Services, LLC is recalling Pramipexole Di-HCl tablets because they may be mislabeled as Multivitamin/Multimineral or Perphenazine.
Aidapak Services is recalling carbamazepine ER tablets that may be mislabeled as acarbose due to a label mixup.
Aidapak Services is recalling Misoprostol tablets that may be mislabeled as Quinapril HCl. The error could lead to patients receiving the wrong medication.
Aidapak Services is recalling Ribavirin capsules that may be mislabeled as Modafinil or Desipramine. The error involves incorrect product identification on the packaging.
Aidapak Services is recalling 20 mg Fosinopril Sodium tablets that may be mislabeled as Tolterodine Tartrate ER capsules.
Aidapak Services, LLC is recalling 10 mg Torsemide tablets because they may be mislabeled as 50 mg Pyridoxine HCl tablets.