Hazard
9,607 recalls in our database tag this hazard, drawn from FDA, USDA FSIS, CPSC, and NHTSA source notices.
Of the 9,607 mis labeling recalls we have scored against our rubric, 160 (2%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 588 (6%) 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 mis labeling 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.
Guerbet LLC is recalling 3,860 Optiray syringes because an RFID formatting error causes the injector to read the product as expired, preventing injection.
Wismettac Asian Foods is recalling Nori Ajitsuke because the label incorrectly lists seafood species. The product contains skipjack tuna and krill.
Guerbet LLC is recalling 3,140 prefilled sodium chloride syringes because an RFID formatting error prevents the Optivantage injector from administering the product.
YOUBITE, LLC is recalling approximately 7,197 pounds of pork and turkey sausage products because they contain natural sheep or pork casings not declared on the label.
Tesla is recalling 2019 Model 3 vehicles because the driver-side sun visor may lack required air bag warning information, increasing injury risk.
Southeastern Grocers is recalling 18-count Variety Pack Cookies made in-store because peanut butter cookies were included without declaring peanuts on the label.
Whole Flower Farms LLC is recalling Oatmeal Chocolate Chip Cookies due to undeclared soy lecithin. The product was distributed in Oregon.
Whole Flower Farms LLC is recalling 27 units of Chocolate Chip Cookies due to undeclared soy lecithin. The product was distributed in Oregon.
Southeastern Grocers is recalling 18-count Peanut Butter Cookies because the ingredient labels failed to declare peanuts.
Whole Flower Farms LLC is recalling Peanut Butter Chocolate Chip Cookies due to undeclared soy lecithin. The product was distributed in Oregon.
Zimmer GmbH is recalling 19 Sidus Stem-Free Shoulder Humeral Head implants due to incorrect size labeling on the packaging.
Implant Direct Sybron Manufacturing is recalling 22 vials of dental implants due to incorrect part numbers on the vial caps.
Implant Direct Sybron Manufacturing is recalling 158 dental implants because the incorrect device was packaged in the vial.
Alkermes is recalling 16,231 Vivitrol kits because 1-inch needles were incorrectly placed in sleeves labeled for 1.5-inch needles. The drug vials are not affected.
Merit Medical Systems is recalling 88 Custom Procedure Kits because they were incorrectly labeled as latex-free.
Merit Medical Systems is recalling 24 Vein Procedure Kits because they were incorrectly labeled as latex-free.
Darmerica, LLC is recalling 1.8 kilograms of bulk Quinacrine Dihydrochloride API because testing revealed the product was actually Artemisinin.
Musculoskeletal Transplant Foundation is recalling nine QuickGraft Model 430PST units because the label measurement was not taken under tension, potentially extending surgical time.
Danone is recalling Silk Soymilk Vanilla Bag-In-Box because the outer box incorrectly identifies the product as almond milk. The internal product is correctly labeled as soymilk.
Arrow International Inc is recalling 231 units of 8.5 Fr. X 16 cm Quad-Lumen Central Venous Catheterization Kits because they may contain the incorrect banner card.
Abbott is recalling 159 APS Accelerator modular systems because the safety pacemaker label is missing. The Operations Manual has been updated to specify a 200 mm minimum safety distance for pacemaker wearers.
Philips is recalling infant/child defibrillator pads due to incorrect age range labeling on the foil packaging.
Getinge is recalling one HEMASHIELD GOLD vascular graft that was incorrectly packed in a carton labeled for a HEMASHIELD PLATINUM graft.
Pfizer is recalling 7,824 bottles of ethosuximide capsules because the expiration date on the label is incorrect.
Pfizer is recalling 7,686 bottles of Zarontin (ethosuximide) capsules because the expiration date on the label is incorrect.