Hazard
145 recalls in our database tag this hazard, drawn from FDA, USDA FSIS, CPSC, and NHTSA source notices.
Of the 145 chemical exposure recalls we have scored against our rubric, 0 (0%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 27 (19%) 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 chemical exposure 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.
Philips Medical Systems is recalling 71 GEMINI TF PET/CT 64 Slice UPS accessory devices due to risks of battery acid leakage, overheating, and fume emission.
Philips Medical Systems is recalling 125 MX 16 Slice UPS accessory devices due to risks of battery acid leakage, overheating, and fume emission.
Philips is recalling 10 Gemini LXL 16 Slice CT systems worldwide due to UPS accessory defects that may cause battery acid leakage, overheating, or fumes.
Philips is recalling 11 MX 16 Slice Phase II CT systems because their UPS accessory devices may leak battery acid, overheat, or emit fumes.
Philips Medical Systems is recalling 215 Ingenuity Core UPS accessory devices due to risks of battery acid leakage, overheating, and fume emission.
Philips is recalling Brilliance CT 40 Uninterruptible Power Supply accessories due to risks of battery acid leakage, overheating, and fume emission.
Philips Medical Systems is recalling AXIS Uninterruptible Power Supply (UPS) accessory devices used with CT and diagnostic imaging systems due to risks of battery acid leakage, overheating, and fume emission.
Philips Medical Systems is recalling 126 UPS accessory devices for CT scanners due to risks of battery acid leakage, overheating, and fume emission.
Philips Medical Systems is recalling three GEMINI TF Ready UPS accessory devices used with CT and diagnostic imaging systems due to risks of battery acid leakage, overheating, and fumes.
Philips Medical Systems is recalling 288 Ingenuity Core 128 UPS accessory devices due to risks of battery acid leakage, overheating, and fume emission.
Philips Medical Systems is recalling two Diamond Select Brilliance CT 16 systems due to a risk of battery acid leakage, overheating, and fumes from the UPS accessory.
Philips Medical Systems is recalling 14 Ingenuity TF UPS accessory devices due to risks of battery acid leakage, overheating, and fume emission.
Philips is recalling 69 GEMINI TF PET/CT 16 Slice systems due to UPS accessory devices that may leak battery acid, overheat, or emit fumes.
Philips Medical Systems is recalling 277 BrightView SPECT UPS accessory devices due to risks of battery acid leakage, overheating, and fume emission.
Philips Medical Systems is recalling 110 iCT SP UPS accessory devices used with CT and diagnostic imaging systems due to risks of battery acid leakage, overheating, and fume emission.
Philips is recalling 25 Brilliance CT 6 Slice Air UPS accessories due to risks of battery acid leakage, overheating, and fume emission.
Philips Medical Systems is recalling 847 UPS accessory devices for CT scanners due to risks of battery acid leakage, overheating, and fume emission.
Philips Medical Systems is recalling 36 Precedence 16 UPS accessory devices used in CT and diagnostic imaging systems due to risks of battery acid leakage, overheating, and fume emission.
Philips is recalling 7 Gemini 16 PET/CT Uninterruptible Power Supply units worldwide due to risks of battery acid leakage, overheating, and fumes.
Philips Medical Systems is recalling 337 BrightView XCT UPS accessory devices due to risks of battery acid leakage, overheating, and fume emission.
Philips Medical Systems is recalling 81 CardioMD III UPS accessory devices for CT and diagnostic imaging systems due to risks of battery acid leakage, overheating, and fume emission.
Philips Medical Systems is recalling 108 BrightView X UPS accessory devices used with CT and diagnostic imaging systems due to risks of battery acid leakage, overheating, and fume emission.
Discus Dental LLC is recalling Relief ACP Oral Care Gel because some units were filled with hydrogen peroxide instead of phosphate gel, potentially causing increased sensitivity.
3M is recalling Steri-Vac Gas Sterilizers due to a rare failure that could cause ethylene oxide exposure. The issue affects specific models manufactured in late 2006 and 2007.
Beckman Coulter is recalling AU2700 and AU5400 Clinical Chemistry Analyzers because tubing connections may leak concentrated detergent.