Hazard
314 recalls in our database tag this hazard, drawn from FDA, USDA FSIS, CPSC, and NHTSA source notices.
Hazard tags are short, machine-readable labels we attach to every recall to make cross-cutting queries possible — “all manufacturing deviation recalls regardless of agency”, “all listeria recalls in California”, “all airbag recalls in 2025”. The tags are extracted from each recall’s source text during the LLM rewrite step and validated against a fixed schema.
A recall can carry multiple tags — a Listeria recall might also be tagged ready-to-eat and undeclared-allergen. Use the full-text search if you want to combine hazard tags with brand or category filters.
CA BOTANA's Doctor. D. Schwab Mineral Sunscreen SPF 50 is being recalled due to manufacturing process deviations. The recall affects 1,167 tubes distributed in CA, CO, FL, PR, and WA.
CA BOTANA International is recalling Elixir by Coco March Mineral Sunscreen SPF 50 due to Current Good Manufacturing Practice (CGMP) deviations. The recall affects 3,295 bottles distributed in CA, CO, FL, PR, and WA.
Doctor D. Schwab Controlling Balm is being recalled due to manufacturing practice deviations. The recall affects 555 tubes distributed in California, Colorado, Florida, Puerto Rico, and Washington.
CA BOTANA International is recalling 805 tubes of Doctor D. Schwab Shimmery Sun Lotion Sunscreen SPF 30 due to manufacturing compliance deviations. The affected product was distributed in California, Colorado, Florida, Puerto Rico, and Washington.
Elixir by Coco March Tinted Mineral Sunscreen SPF 50 is being recalled by CA BOTANA International, Inc. due to manufacturing practice deviations. The recall affects products distributed in California, Colorado, Florida, Puerto Rico, and Washington.
DermaRite Industries recalls 4-N-1 Skin Protectant nationwide due to manufacturing facility contamination. Consumers should stop using the product.
Skin Protectant with Lanolin, manufactured by DermaRite Industries, is being recalled due to CGMP violations and contamination detected in other products at the same manufacturing facility. Nationwide distribution; 5,876 units affected.
FarmaKeio Outsourcing LLC is recalling testosterone and triamcinolone acetonide subcutaneous pellets due to potential metal particulate matter from manufacturing deviations. The recall affects 21,324 pellets distributed nationwide and in Antigua.
Major Pharmaceuticals is recalling Chlorpromazine Hydrochloride 50 mg tablets nationwide due to presence of N-Nitroso Desmethyl Chlorpromazine above recommended intake limits, affecting 506 blister packs (lots N02009 and N02026).
Quick Touch Alcohol Prep Pads (70% isopropyl alcohol) are being voluntarily recalled due to Current Good Manufacturing Practice deviations. The recall affects 500 cases with Lot #20240610, expiration June 2029.
Zydus Pharmaceuticals is recalling Chlorpromazine Hydrochloride tablets nationwide due to manufacturing deviations resulting in N-Nitroso Desmethyl Chlorpromazine exceeding FDA acceptable intake limits. Affected lots are Z403011 and Z407335.
Zydus Pharmaceuticals is recalling chlorpromazine hydrochloride 25 mg tablets nationwide due to the presence of N-Nitroso Desmethyl Chlorpromazine above acceptable limits. No illnesses have been reported.
Zydus Pharmaceuticals recalls Chlorpromazine Hydrochloride 200 mg tablets nationwide due to N-Nitroso Desmethyl Chlorpromazine exceeding recommended acceptable limits. No illnesses reported.
KABANA SKIN CARE is recalling In Your Face Mineral Tint SPF 31 sunscreen due to Current Good Manufacturing Practice (cGMP) deviations. The voluntary recall affects 76 bottles distributed in New Jersey, Florida, and Michigan.
Erin's Faces Mineral SPF 32 Sunscreen (54 tubes, Lot 410-002) is being recalled due to manufacturing practice deviations. The product was distributed in New Jersey, Florida, and Michigan.
Torrent Pharma Inc. is recalling 972 cartons of Fluoxetine 20 mg tablets nationwide due to manufacturing deviations resulting in N-Nitroso Fluoxetine exceeding acceptable intake limits. Patients should contact their healthcare provider or pharmacist.
Amerisource Health Services is recalling 21 cartons of Indomethacin Extended-Release Capsules due to manufacturing deviations. Patients should consult their pharmacist before using this prescription medication.
Rapidol triple antibiotic ointment (lot SP27A, expiring 09/30/2026) distributed in Delaware and North Carolina was recalled for manufacturing practice deviations. The voluntary recall was initiated April 24, 2025, and terminated February 19, 2026.
The FDA is recalling Maximum Security Anticavity Gel Toothpaste sachets distributed in Delaware and North Carolina due to manufacturing practice deviations at the producer facility.
Anticavity toothpaste containing sodium fluoride is being recalled due to manufacturing deviations. The recall affects 391,680 tubes distributed in Delaware and North Carolina.
BRS Analytical Services is recalling Carboxymethylcellulose Sodium 0.5% ophthalmic solution nationwide due to manufacturing practice deviations and inability to assure sterility. Multiple lot numbers are affected.
Preferred Pharmaceuticals, Inc. is recalling 1190 bottles of Clindamycin Hydrochloride Capsules nationwide due to manufacturing practice deviations. The product was manufactured by Glenmark Pharmaceuticals Limited.
Pharmadel is recalling Urodel, a homeopathic urinary tract infection relief tablet, due to manufacturing practice violations. The recall affects 10,752 bottles distributed in Delaware.
Apipharma is voluntarily recalling Hemopropin Ointment due to manufacturing process deviations. Approximately 4,218 boxes distributed in Arizona are affected.
The FDA has recalled Rapidol Arnica Gel, a topical homeopathic medicine, due to deviations from good manufacturing practices. No illnesses or injuries have been reported.