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
Synergy Rx is recalling Betamethasone 0.25% cream because it may not be sterile. The recall covers all lots distributed nationwide.
Synergy Rx is recalling DUO Cream because the product lacks assurance of sterility and has CGMP deviations. The recall covers all lots distributed nationwide.
Synergy Rx is recalling Fluorouracil creams because of a lack of assurance of sterility and CGMP deviations.
Synergy Rx is recalling Lactic Acid Solution in all strengths due to a lack of assurance of sterility and CGMP deviations.
Synergy Rx is recalling Cantharidin 0.7% Solution and Cantharidan/Podophyllum Solution due to lack of assurance of sterility and CGMP deviations.
Teva Pharmaceuticals is recalling specific lots of Buprenorphine and Naloxone Sublingual Tablets because they failed impurity and degradation specifications.
Synergy Rx is recalling Gentle Supreme Bleaching Cream because the product lacks assurance of sterility and has CGMP deviations.
Synergy Rx is recalling QUAD PEEL chemical peels nationwide due to a lack of assurance of sterility and CGMP deviations.
Synergy Rx is recalling Enhanced Retin Anti-Wrinkle Cream products due to a lack of assurance of sterility and CGMP deviations.
Synergy Rx is recalling Diclofenac Lip Balm products because they may not be sterile. The recall covers all lots distributed nationwide.
Synergy Rx is recalling Azelaic Acid 15% Cream because the product lacks assurance of sterility and has CGMP deviations.
Synergy Rx is recalling Kojic Acid 8%/Azelaic Acid 15% Cream because it lacks assurance of sterility and has CGMP deviations.
Synergy Rx is recalling MALEK'S MAGIC prescription cream because it lacks assurance of sterility and has CGMP deviations.
Synergy Rx is recalling Erythromycin 2% in CeraVe Cream and Erythromycin 3% / Retinoic Acid 0.05% due to lack of assurance of sterility and CGMP deviations.
Synergy Rx is recalling Rosacea Cream because the product lacks assurance of sterility and has CGMP deviations.
Synergy Rx is recalling HI-LITE Cream because the product lacks assurance of sterility and has CGMP deviations.
Synergy Rx is recalling Calming Cream (Hydrocortisone 2.5%) because the product lacks assurance of sterility and has CGMP deviations.
Synergy Rx is recalling Brightening Cream due to a lack of assurance of sterility and CGMP deviations. The product is distributed nationwide.
Synergy Rx is recalling various retinoic acid products due to a lack of assurance of sterility and CGMP deviations.
Synergy Rx is recalling all lots of CLEAR (Benzoyl Peroxide 3.75%, Clindamycin 1.2% Gel) due to a lack of assurance of sterility and CGMP deviations.
Synergy Rx is recalling Clobetasol 0.05% products because the FDA identified a lack of assurance of sterility and CGMP deviations.
Isomeric Pharmacy Solution is recalling 6,999 vials of Triamcinolone 40 mg/mL injection due to Current Good Manufacturing Practice (CGMP) deviations.
Synergy Rx is recalling all lots of Ketoconazole 2%/Hydrocortisone 1.5% Cream because the product lacks assurance of sterility and has CGMP deviations.
Synergy Rx is recalling Human Chorionic Gonadotropin tablets because the product lacks assurance of sterility and has CGMP deviations.
Synergy Rx is recalling Urea 40% Cream because it may not be sterile and has CGMP deviations.