Hazard
536 recalls in our database tag this hazard, drawn from FDA, USDA FSIS, CPSC, and NHTSA source notices.
Of the 536 regulatory non compliance recalls we have scored against our rubric, 0 (0%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 56 (10%) 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 non compliance 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.
Exactech is recalling two Novation Ceramic AHS Cluster-Hole Shell acetabular cups because they were packaged before regulatory approval.
Exactech is recalling nine Novation femoral stems because they were packaged before receiving FDA approval for a site change.
Exactech is recalling three Novation Ceramic AHS Cluster-Hole Shells because they were packaged before the required site-change approval was granted.
Exactech is recalling one Novation femoral stem device because it was packaged before the required FDA site-change approval was granted.
Medscience Inc is recalling AllergiEnd ST-9 skin test applicators and trays because they were marketed without FDA clearance.
Nubreed Nutrition is voluntarily recalling all lot codes of Undisputed dietary supplements because they contain Acacia rigidula, an ingredient that does not meet FDA dietary ingredient definitions.
Nubreed Nutrition is voluntarily recalling Undisputed dietary supplements because they contain Acacia rigidula, an ingredient that does not meet FDA dietary ingredient definitions.
Northeast Laboratory Services is recalling 9,300 units of GBS Medium because the product was marketed without FDA 510(k) clearance.
Northeast Laboratory Services is recalling 11,720 units of GBS Medium tubes because they were marketed without FDA 510(k) clearance.
Medtronic Navigation is recalling four BioTex Reusable Adapter Kits because they were distributed without FDA 510(k) clearance.
Faye's Texas Naturals is recalling 1,140 jars of Chili Petin Picante Caliente because pH levels were not tested as required by acidified food regulations.
Faye's Texas Naturals is recalling 1,979 jars of Chili Petin Corn Relish because pH levels were not tested as required by acidified food regulations.
Faye's Texas Naturals is recalling 816 jars of Chili Petin Picante Muy Caliente because pH levels were not tested as required by acidified food regulations.
Faye's Texas Naturals is recalling 65 bottles of Chili Petin Pepper Sauce because pH levels were not tested as required by acidified food regulations.
Sunset Natural Products Inc. is recalling Venocell dietary supplements pursuant to a consent decree requiring the destruction of products manufactured or distributed since April 2, 2014.
Sunset Natural Products is recalling Chardon de Marie dietary supplements pursuant to a consent decree requiring the destruction of products manufactured since April 2014.
Sunset Natural Products Inc. is recalling Hepasil dietary supplements under a consent decree requiring the destruction of products distributed since April 2, 2014.
Sunset Natural Products Inc. is recalling Prostax Forte dietary supplements pursuant to a consent decree requiring the destruction of products manufactured or distributed since April 2, 2014.
Sunset Natural Products Inc. is recalling 4,000 bottles of Prostamax DUO dietary supplements in Florida and Nevada pursuant to a consent decree.
Sunset Natural Products Inc. is recalling Neuro-Cetin dietary supplements under a consent decree requiring the destruction of products manufactured since April 2014.
Sunset Natural Products is recalling Abee Med dietary supplements under a consent decree requiring the destruction of products manufactured since April 2014.
Sunset Natural Products is recalling Prostaliv dietary supplements pursuant to a consent decree requiring the destruction of products manufactured or distributed since April 2, 2014.
Garden Harvest is recalling House MADE Sriracha Sauce because the firm was manufacturing acidified foods without a license.
Garden Harvest is recalling 153 cases of Roasted Mediterranean Pepper Relish because the firm was manufacturing acidified foods without a license.
Garden Harvest is recalling 160 cases of Cleveland Pickle Spicy Garlic Dill because the firm was manufacturing acidified foods without a license.