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.
Airwair is recalling Dr. Martens Vegan 1460 boots in cherry red because the tongue lining contains benzidine. Consumers should stop using the boots and contact Dr. Martens for a refund or replacement.
Sorin Group USA is recalling 7,546 STOCKERT Heater-Cooler Systems 3T because plastic fibers may allow hydrogen peroxide to diffuse into the blood compartment.
Sorin Group USA is recalling 7,546 STOCKERT Heater-Cooler Systems 3T because plastic fibers may allow excessive hydrogen peroxide to diffuse into the blood compartment.
Sorin Group USA is recalling 7,546 STOCKERT Heater-Cooler Systems because plastic fibers may allow excessive hydrogen peroxide to diffuse into the blood compartment.
Sorin Group USA is recalling 7,546 STOCKERT Heater-Cooler Systems 3T because plastic fibers may allow excessive hydrogen peroxide to diffuse into the blood compartment.
Sorin Group USA is recalling STOCKERT Heater-Cooler System 3T units because plastic heat exchanger fibers may allow excessive hydrogen peroxide diffusion.
Sorin Group USA is recalling 7,546 STOCKERT Heater-Cooler Systems because plastic fibers may allow hydrogen peroxide to diffuse into the blood compartment.
CareFusion is recalling 384,923 units of the SmartSite Add-On Bag Access Device because the spike port may separate or leak, potentially interrupting medication infusion.
Moose Toys is recalling Little Live Pets Lil Frog toys because the battery cap can become a projectile and chemicals can leak, causing eye irritation.
Bausch + Lomb is recalling PeroxiClear Peroxide Solution because the product was found to contain excess residual levels of hydrogen peroxide.
Draeger Medical is recalling D-Vapor and D-Vapor 3000 anesthesia vaporizers because they may release desflurane during filling, posing an eye irritation risk.
3M is recalling 74 Steri-Vac Gas Sterilizer valves due to a labeling error that could cause incorrect installation and potential valve failure.
DeRoyal Industries is recalling 355 sterile surgical kits containing 3M DuraPrep solution due to unintended exposure to sterilant during package sterilization.
DeRoyal Industries is recalling specific lots of sterile surgical kits containing 3M DuraPrep solution due to unintended exposure to sterilant during the sterilization process.
Philips Medical Systems is recalling Extended Brilliance Workstation UPS accessory devices due to risks of battery acid leakage, overheating, and fume emission.
Philips is recalling 15 Gemini GXL 16 Slice CT systems worldwide because their UPS accessory devices may leak battery acid, overheat, or emit fumes.
Philips Medical Systems is recalling 23 Ingenuity Flex 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 Precedence 6 UPS accessory devices for CT and diagnostic imaging systems due to risks of battery acid leakage, overheating, and fume emission.
Philips is recalling 31 TruFlight Select PET/CT systems because the Uninterruptible Power Supply (UPS) accessory devices may leak battery acid, overheat, or emit fumes.
Philips is recalling 156 Ingenuity CT Uninterruptible Power Supply (UPS) accessory devices due to a risk of battery acid leakage, overheating, and fume emission.
Philips Medical Systems is recalling 10 FORTE 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 11 Forte-JetStream AZ UPS accessory devices used in CT and diagnostic imaging systems due to risks of battery acid leakage, overheating, and fumes.
Philips Medical Systems is recalling Brilliance iCT UPS accessory devices due to risks of battery acid leakage, overheating, and fume emission.
Philips Medical Systems is recalling 39 GEMINI TF Big Bore UPS accessory devices due to risks of battery acid leakage, overheating, and fume emission.
Philips Medical Systems is recalling nine Ingenuity PET/MR Uninterruptible Power Supply (UPS) accessory devices due to risks of battery acid leakage, overheating, and fume emission.