Hazard
91 recalls in our database tag this hazard, drawn from FDA, USDA FSIS, CPSC, and NHTSA source notices.
Of the 91 regulatory violation recalls we have scored against our rubric, 1 (1%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 43 (47%) 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 regulatory violation 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.
Garden Harvest is recalling RJ's Peppers in Oil because the firm was manufacturing acidified foods without a license.
Keim's Garden Harvest is recalling pickled zesty mustard eggs because the firm was manufacturing acidified foods without a license.
Vigil's Beef Jerky Co. is recalling approximately 48 pounds of beef jerky produced without federal inspection but marked as inspected.
Advanced Photonic Systems is recalling 235 Luxurian devices because they were marketed without FDA clearance or approval.
ChiroNutraceutical LLC is recalling Chirothin dietary supplement bottles because the product contains unapproved human chorionic gonadotropin (hCG) and was marketed without an approved NDA or ANDA.
LumiQuick Diagnostics Inc. is recalling all lots of the Adenovirus Antigen Test Card because they were shipped to locations without approved FDA applications.
LumiQuick Diagnostics Inc. is recalling Fecal Occult Blood Test Cards because they were shipped to locations without approved FDA applications or clearances.
LumiQuick Diagnostics Inc. is recalling its Drugs of Abuse Panel Test Device because it was shipped to locations without required FDA approvals.
LumiQuick Diagnostics Inc. is recalling Malaria pan Antigen Tests because they were shipped to US locations without approved PMA, IDE, or 510(k) clearance.
LumiQuick Diagnostics is recalling K2 Test Cards because they were shipped to locations without required FDA clearances.
LumiQuick Diagnostics Inc. is recalling Tuberculosis Antibody Test Card Serum because it was shipped to locations without required FDA clearances.
AMS Diagnostics is recalling 167 BUN Urea Nitrogen kits because they were marketed outside FDA 510(k) requirements.
AMS Diagnostics is recalling 13 Uric Acid test kits because they were marketed outside FDA 510(k) requirements.
Kabco Pharmaceuticals is recalling Perfect 3000 Vanilla Powder because it was distributed in violation of a federal consent decree.
Kabco Pharmaceuticals is recalling 681.60 kg of Perfect 3000 Chocolate Powder distributed in New York in violation of a federal consent decree.
Prosperity Resources International is recalling Golden Flower Dried Ginger in New York State due to violations of the Agriculture and Markets Law.