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.
Sunset Natural Products Inc. is recalling Performens dietary supplements pursuant to a consent decree requiring the destruction of products manufactured or distributed since April 2014.
Sunset Natural Products Inc. is recalling Asey Dietary Supplement pursuant to a consent decree requiring the destruction of products manufactured or distributed since April 2, 2014.
Sunset Natural Products Inc. is recalling Growlean Dietary Supplement pursuant to a consent decree requiring the destruction of products manufactured or distributed since April 2014.
Sunset Natural Products Inc. is recalling Triphala Dietary Supplement pursuant to a consent decree requiring the destruction of products manufactured or distributed since April 2, 2014.
Sunset Natural Products Inc. is recalling Blanc Dietary Supplement pursuant to a consent decree requiring the destruction of products manufactured or distributed since April 2, 2014.
Sunset Natural Products Inc. is recalling Vital Cure dietary supplements pursuant to a consent decree requiring the destruction of products manufactured since April 2014.
Sunset Natural Products Inc. is recalling Prostax Forte dietary supplements pursuant to a consent decree requiring the destruction of products manufactured since April 2014.
Midwest International Corp is recalling low acid canned fish products that lack a registered manufacturer and scheduled process. The recall covers distribution in eight states.
Midwest International Corp is recalling dried vegetable products because they are acidified foods without a registered manufacturer or scheduled process.
Ultroid Technologies is recalling 62 mobile generator units and sterile probes because they were not manufactured under required quality system controls.
Midwest International Corp is recalling Dai Yu Hairtail because it is an acidified food without a registered manufacturer and scheduled process.
Northridge Tri-Modality Imaging is recalling three TriFoillmaging Triumph/Triumph II Research CT scanners because they may not meet federal X-ray safety standards.
Philips is recalling 15 DuraDiagnost stationary X-ray systems because the monitor allows users to mute the exposure beep and the tabletop is missing required safety labels.
Siemens is recalling 76 RAPIDPoint 500 software upgrade kits because some include a dialysate mode not cleared for shipment in the United States.
Pentax Medical is recalling the EPK-i5010 Video Processor because it was shipped with a water bottle assembly not cleared for use in the United States.
Pentax Medical is recalling Video Processor EPK-i5010 units because they were shipped with a water bottle assembly not cleared for use in the United States.
Pentax Medical is recalling the EPK-i5010 Video Processor because it was shipped with a water bottle assembly not cleared for use in the United States.
Pentax Medical is recalling the EPK-i5010 Video Processor because it was shipped with a water bottle assembly not cleared for use in the United States.
U.S. Cado Holdings is recalling approximately 29,645 pounds of imported frozen Swai fillets that entered U.S. commerce without meeting federal residue testing requirements.
Lifeline First Aid LLC is recalling Cadillac First Aid Kits because they contain a CPR mask cleared only for prescription use, not over-the-counter.
Ergoactives is recalling 278 HeaterBaum Foot & Ankle Heating Pads because they were marketed without a cleared 510(k).
ZYTO Technologies is voluntarily recalling ZYTO Tower devices and software because their marketing claims exceeded the scope of their FDA 510(k) clearance.
U.S. Cado Holdings is recalling approximately 27,995 pounds of imported frozen Swai fillets that entered U.S. commerce without meeting federal residue testing requirements.
Miami Fat Supply is recalling 443 Red Head 2 Reusable Fat Harvesting Canisters because they were marketed without FDA clearance and are not approved for multiple use.
Exactech is recalling one Novation femoral stem device because it was packaged before the required site-change approval was granted.