Hazard
2,383 recalls in our database tag this hazard, drawn from FDA, USDA FSIS, CPSC, and NHTSA source notices.
Of the 2,383 sterility recalls we have scored against our rubric, 1 (0%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 2,113 (89%) are Severe.
Which agencies issued them
Hazard tags are short, machine-readable labels we attach to every recall to make cross-cutting queries possible — “all sterility 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.
Wells Pharmacy Network LLC is recalling 526 vials of compounded Nandrolone Decanoate injectable nationwide due to a lack of assurance of sterility.
Tri-Coast Pharmacy is recalling 17 vials of TriMix injection because the agency could not ensure the products were sterile.
Wells Pharmacy Network LLC is recalling B-complex + Vit C injectable vials due to a lack of assurance of sterility.
Wells Pharmacy Network LLC is recalling compounded Chorionic Gonadotropin injectable kits due to a lack of assurance of sterility.
Wells Pharmacy Network LLC is recalling 908 compounded Chorionic Gonadotropin Injectable Kits nationwide due to a lack of assurance of sterility.
Wells Pharmacy Network LLC is recalling 2,339 compounded Chorionic Gonadotropin Injectable Kits nationwide due to a lack of assurance of sterility.
Colonia Care Pharmacy is recalling C-PAV/PHENTOL/PGE1 injectable drug products due to lack of assurance of sterility. The recall affects products distributed in New Jersey and New York.
Colonia Care Pharmacy is recalling C-PAV/PHENTOL/ATROP/PGE1 injectable products due to lack of assurance of sterility. The recall affects products distributed in New Jersey and New York.
Amgen is recalling 11,434 vials of Kyprolis (carfilzomib) injection because potential cracks in the glass vials may compromise sterility.
Cantrell Drug Company is recalling 471 bags of Fentanyl Citrate 1,500 mcg in 0.9% Sodium Chloride due to a lack of assurance of sterility.
Cantrell Drug Company is recalling 162 syringes of Lidocaine HCl 1% because the firm cannot assure the sterility of the product.
Cantrell Drug Company is recalling 1,494 syringes of Heparin Sodium due to a lack of assurance of sterility. The products were distributed nationwide.
Cantrell Drug Company is recalling 645 vials of Calcium Chloride Injection Solution because the firm cannot assure the sterility of the product.
Cantrell Drug Company is recalling 37 syringes of Midazolam HCl 50 mg/50 mL due to a lack of assurance of sterility. The product was distributed nationwide.
Cantrell Drug Company is recalling 2,509 single-dose Hydromorphone HCl syringes nationwide due to a lack of assurance of sterility.
Cantrell Drug Company is recalling specific lots of Fentanyl Citrate and Bupivacaine HCl bags due to a lack of assurance of sterility.
Cantrell Drug Company is recalling 1,748 bags of Morphine Sulfate 1 mg/mL due to a lack of assurance of sterility. The product was distributed nationwide.
Cantrell Drug Company is recalling 2,681 bags of Oxytocin 30 USP Units due to a lack of assurance of sterility. The affected product is distributed nationwide.
Fallon Wellness Pharmacy is recalling 10 vials of PAPA/PHEN/PROST injection due to environmental monitoring excursions that raise concerns about sterility assurance.
North American Rescue LLC is recalling Range Trauma Kit Hardcases because the manufacturer has concerns about the sterility of the eye wash irrigating solution included in the kits.
Fallon Wellness Pharmacy is recalling 5 vials of PAPA/PHEN/PROST injection due to environmental monitoring excursions that raise concerns about sterility assurance.
North American Rescue LLC is recalling Mini Resupply Trauma Kits because the manufacturer has concerns about the sterility of the included eye wash solution.
North American Rescue LLC is recalling Aid Backpack Kits because the manufacturer has concerns about the sterility of the eye wash irrigating solution.
North American Rescue LLC is recalling USCG Boat Response Kits because the manufacturer has concerns about the sterility of the eye wash irrigating solution.
North American Rescue LLC is recalling K-9 Trauma Field Kits because the manufacturer has concerns about the sterility of the included eye wash irrigating solution.