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
Michigan Herbal Remedies is recalling 25 bottles of 300mg CBD hemp oil because the product contains elevated levels of undeclared lead.
Michigan Herbal Remedies is recalling 50 bottles of BC Hemp Co. CBD Oil due to elevated levels of undeclared lead.
Vilvet Pharmaceuticals is voluntarily recalling 1,716 bottles of VILEVEV MB Urinary Antiseptic due to current Good Manufacturing Practice (cGMP) deviations.
Vilvet Pharmaceuticals is recalling 11,640 bottles of VILAMIT MB capsules due to current Good Manufacturing Practice (cGMP) deviations. The recall is voluntary and nationwide.
UVT INC is recalling Saniderm Advanced Hand Sanitizer because it contains undeclared methanol. The product was distributed nationwide in the USA.
Polarized LLC is recalling Saniderm Advanced Hand Sanitizer because it contains undeclared methanol and less ethanol than labeled.
MasterPharm LLC is recalling 600 capsules of Progesterone (Modified Release) 150 mg due to a lack of processing controls.
Lupin Pharmaceuticals is recalling specific bottles of 10 mg Lisinopril tablets because 20 mg tablets were found inside. Consumers should stop using the affected product.
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 543 units of Formula 82M topical solution nationwide because the product lacks assurance of conformity to specifications.
MasterPharm LLC is recalling Progesterone 300 mg Troches because the product lacks assurance of conformity to specifications.
MasterPharm LLC is recalling Sildenafil 50 mg Troches nationwide due to a lack of processing controls that ensures 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 specific lots of Progesterone 150 mg tablets because they lack assurance of 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 Estriol 8 mg capsules nationwide due to a lack of processing controls that ensures conformity to specifications.
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.
Sun Pharmaceutical is recalling Clonazepam Orally Disintegrating Tablets because routine stability testing detected cross-contamination with clozapine.
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 Tadalafil 26 mg capsules nationwide due to a lack of processing controls that ensures conformity to 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 Vardenafil 20 mg Troches nationwide due to a lack of processing controls that ensures conformity to specifications.
Allergan is recalling specific lots of Skin Medica Acne Treatment Lotion because the products failed potency tests at 12 and 24 months.
MasterPharm LLC is recalling Yohimbine HCL 5.4mg capsules nationwide due to a lack of processing controls that ensures conformity to specifications.