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 Omeprazole/Sodium Bicarbonate capsules because they may be mislabeled as Cyanocobalamin or Omega-3 fatty acid products.
Aidapak Services is recalling Calcium Citrate tablets that may be mislabeled as Tizanidine HCl. The error could lead to patients taking the wrong medication.
Aidapak Services, LLC is recalling Quetiapine Fumarate 25 mg tablets because they may be mislabeled as Chlordiazepoxide HCl capsules.
Aidapak Services, LLC is recalling Itraconazole capsules because they may be mislabeled as Famciclovir tablets. The error could lead to patients receiving the wrong medication.
Aidapak Services, LLC is recalling 402 Metoprolol Tartrate tablets because they may be mislabeled as Docusate Sodium capsules.
Aidapak Services, LLC is recalling D-Alpha Tocopheryl Acetate capsules because they may be mislabeled as Cyanocobalamin tablets.
Aidapak Services, LLC is recalling Metoprolol Succinate ER 200 mg tablets due to a potential labeling mixup. The affected repacked drugs were distributed in four western states.
Aidapak Services is recalling Omeprazole/Sodium Bicarbonate capsules because they may be mislabeled as Benzocaine/Menthol lozenges. The FDA classifies this as a Class II recall.
Aidapak Services, LLC is recalling Hydralazine HCL 25 mg tablets because they may be mislabeled as Docusate Calcium 240 mg capsules.
Aidapak Services is recalling Rifaximin 200 mg tablets that may be mislabeled as Toprol 25 mg. The repacked drugs were distributed in four western states.
Aidapak Services is recalling Quetiapine Fumarate 25 mg tablets because they may be mislabeled as multivitamin or aspirin products.
Aidapak Services is recalling Solifenacin Succinate 5 mg tablets because they may be mislabeled as Bromocriptine Mesylate 2.5 mg.
Aidapak Services, LLC is recalling Benzoicaine/Menthol lozenges because they may be mislabeled as Cholecalciferol/Calcium/Phosphorus tablets.
Aidapak Services, LLC is recalling specific lots of Colchicine 0.6 mg tablets because they may be mislabeled as other medications.
Aidapak Services is recalling Galantamine HBr ER capsules because they may be mislabeled as Famotidine tablets.
Aidapak Services, LLC is recalling Pseudoephedrine HCL 60 mg tablets because they may be mislabeled as Repaglinide 1 mg tablets.
Pfizer is recalling specific lots of Zithromax (azithromycin) injection due to out-of-specification results for a degradant.
Aidapak Services, LLC is recalling Allopurinol 300 mg tablets because they may be mislabeled as Cholecalciferol 400 units.
Aidapak Services is recalling RANOLAZINE ER 500 mg tablets because they may be mislabeled as other medications. The repacked drugs were distributed in four western states.
Aidapak Services is recalling diphenhydramine HCl tablets because they may be mislabeled as atorvastatin, prenatal vitamins, or venlafaxine.
Aidapak Services is recalling Olanzapine 7.5 mg tablets due to a potential labeling mixup with Nortriptyline HCL capsules.
Aidapak Services, LLC is recalling 1 mg Melatonin tablets that may be mislabeled as Omega-3 fatty acid capsules. The error involves a potential mix-up between two different products.
Aidapak Services, LLC is recalling 229 capsules of carbamazepine ER 200 mg due to a labeling mixup where the product may be mislabeled as acamprosate calcium.
Aidapak Services is recalling 200 mg Guaifenesin tablets that may be mislabeled as Pancrelipase DR capsules. The repacked drugs were distributed in Arizona, California, Oregon, and Washington.
Aidapak Services is recalling Omeprazole/Sodium Bicarbonate capsules because they may be mislabeled as Lactobacillus GG or Pyridoxine HCL.