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
MasterPharm LLC is recalling 600 capsules of Progesterone Modified Release 100 mg due to a lack of processing controls that ensures conformity to specifications.
MasterPharm LLC is recalling D-Biotin 300 mg capsules nationwide due to a lack of processing controls that ensures conformity to specifications.
MasterPharm LLC is recalling Sildenafil 50 mg Troches nationwide due to a lack of processing controls that ensures conformity to specifications.
MasterPharm LLC is recalling Progesterone 300 mg Troches because the product lacks assurance of conformity to specifications.
MasterPharm LLC is recalling Progesterone Modified Release 200 mg Capsules because the company lacks processing controls to ensure the product meets specifications.
MasterPharm LLC is recalling 24 grams of Calcium citrate tetrahydrate USP powder due to a lack of processing controls that ensures conformity to specifications.
MasterPharm LLC is recalling 462 units of Formula 82F topical solution due to a lack of processing controls that compromised product specifications.
MasterPharm LLC is recalling specific lots of Progesterone 200 mg Troches nationwide due to a lack of processing controls that ensures conformity to specifications.
MasterPharm LLC is recalling Tadalafil 12 mg capsules nationwide due to a lack of processing controls that ensures conformity to specifications.
MasterPharm LLC is recalling specific lots of Progesterone 150 mg tablets because they lack assurance of conformity to specifications.
MasterPharm LLC is recalling Yohimbine HCL 5.4mg capsules nationwide due to a lack of processing controls that ensures conformity to specifications.
MasterPharm LLC is recalling Testosterone/Anastrozole Pellets 100/6 mg due to a lack of processing controls that ensures conformity to specifications.
MasterPharm LLC is recalling Estriol 6 mg capsules nationwide due to a lack of processing controls that ensures conformity to specifications.
MasterPharm LLC is recalling Tadalafil 18 mg capsules nationwide due to a lack of processing controls that ensures conformity to specifications.
MasterPharm LLC is recalling 543 units of Formula 82M topical solution nationwide because the product lacks assurance of conformity to specifications.
World Event Promotions, LLC is recalling Handese Advanced Instant Hand Sanitizer because the product was found to be subpotent and has high pH levels.
MasterPharm LLC is recalling Progesterone 50 mg Modified Release Capsules nationwide due to a lack of processing controls that ensures conformity to specifications.
MasterPharm LLC is recalling Tadalafil 7 mg capsules nationwide due to a lack of processing controls that ensures conformity to specifications.
MasterPharm LLC is recalling Estriol 8 mg capsules nationwide due to a lack of processing controls that ensures conformity to specifications.
MasterPharm LLC is recalling Minoxidil/Biotin 1.25mg/5mg capsules nationwide due to a lack of processing controls that ensures conformity to specifications.
MasterPharm LLC is recalling specific lots of Progesterone 150 mg Troches nationwide due to a lack of processing controls that ensures conformity to specifications.
Allergan is recalling 8,555 Skin Medica Acne System kits nationwide because the products failed potency tests at 12 and 24 months.
Transliquid Technologies is recalling Mystic Shield hand sanitizer bottles due to the presence of undeclared methanol.
Lupin Pharmaceuticals is recalling Cefdinir for Oral Suspension due to out-of-specification assay results in retention samples.
Walker Emulsions Inc. is recalling 1-gallon bottles of 60% hand sanitizer because it contains an unapproved excipient, DA-2I Ethanol.