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 deaths or serious injuries are reported, 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
Nora Apothecary and Alternative Therapies, Inc. is recalling Methylcobalamin Injections due to FDA inspection findings regarding quality control and lack of assurance of sterility.
Nora Apothecary and Alternative Therapies, Inc. is recalling HCG Inj 1200un/ml MDV products due to FDA inspection findings regarding quality control and lack of assurance of sterility.
Nora Apothecary and Alternative Therapies, Inc. is recalling Tobramycin Ophthalmic Solution due to FDA inspection findings regarding quality control and lack of assurance of sterility.
Nora Apothecary is recalling Vancomycin Ophthalmic Solution because FDA inspections raised concerns about quality control and sterility assurance.
Nora Apothecary and Alternative Therapies, Inc. is recalling Methylcobalamin Injections due to FDA inspection findings regarding quality control and lack of assurance of sterility.
Nora Apothecary and Alternative Therapies, Inc. is recalling Pyridoxine 100mg/ml Injections due to FDA inspection findings regarding quality control and lack of assurance of sterility.
Nora Apothecary and Alternative Therapies, Inc. is recalling HCG Inj 500un/ml MDV, 5 ml Subcutaneous due to FDA inspection findings regarding quality control and lack of assurance of sterility.
Nora Apothecary is recalling Bimix Inj 30:1 MDV penile injections because FDA inspections raised concerns about quality control and sterility assurance.
Nora Apothecary is recalling Meperidine 100mg/ml MDV, 5ml vials due to FDA inspection findings regarding quality control and lack of assurance of sterility.
Nora Apothecary is recalling Vancomycin Ophthalmic Solution because FDA inspections raised concerns about quality control and sterility assurance.
Nora Apothecary and Alternative Therapies, Inc. is recalling Hydroxyprogesterone Inj 250mg/ml MDV, 5 ml Intramuscular due to FDA inspection findings regarding quality control and lack of assurance of sterility.
Nora Apothecary and Alternative Therapies, Inc. is recalling 7 units of Dexamethasone Opth Soln 0.1% PF due to lack of assurance of sterility identified during an FDA inspection.
Nora Apothecary is recalling 72 units of Trimix Penile Injection nationwide due to FDA inspection findings regarding quality control and lack of assurance of sterility.
Nora Apothecary is recalling Trimix penile injections because FDA inspections raised concerns about quality control and sterility assurance.
Nora Apothecary is recalling PHMB Ophthalmic Solution 0.02% because FDA inspections raised concerns about quality control and sterility assurance.
Nora Apothecary and Alternative Therapies, Inc. recalled HCG injection products because FDA inspection findings raised concerns about quality control and sterility assurance. The products were distributed nationwide.
Nora Apothecary is recalling Trimix penile injections because FDA inspections raised concerns about quality control and the assurance of sterility.
Lloyd Inc. of Iowa is recalling Levothroid (levothyroxine sodium) tablets due to cGMP deviations and stability failures. The recall covers specific lots distributed nationwide and to Puerto Rico.
Lloyd Inc. of Iowa is recalling 5.7 million Thyro-Tab tablets because stability failures in previous lots make it impossible to verify the quality of the current lots.
Lloyd Inc. of Iowa is recalling bulk Thyro-Tab tablets due to cGMP deviations and stability failures. The product was distributed to Forest Laboratories for repackaging.
Lloyd Inc. of Iowa is recalling bulk Thyro-Tab 0.175 mg tablets due to cGMP deviations and stability failures. The product was distributed to Forest Laboratories for repackaging.
King Legacy is recalling Levoxyl tablets because they were below specification for potency at the expiry stability point.
King Legacy is recalling Levoxyl tablets because they were below specification for potency at the expiry stability point.
Performance Plus Marketing is recalling BLUE Diamond Platinum Capsules because they may contain undeclared sildenafil, tadalafil, and analogues, making them unapproved drugs.
Performance Plus Marketing, Inc. is recalling Blue Diamond Pill male sexual enhancement products because they may contain undeclared sildenafil, tadalafil, and analogues.