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.
Food and Beverage Inc. is recalling Trader Joe's Peanut Butter Sutter's Formula Cookies because they were packed in Chocolate Chip Cookie bags, posing a peanut allergy risk.
Merit Medical Systems is recalling 44 custom dialysis kits because they contain 2-cuff catheters incorrectly configured and labeled as 1-cuff products.
Weis Markets is recalling Dried Beef Party Rye Dip because the label failed to list egg and milk, which are present in the ingredients.
Centurion Medical Products is recalling Neonatal IV Access Sets because the PVP Prep Pad does not meet required iodine levels for shelf life.
Pine Pharmaceuticals is recalling 136 units of Brilliant Blue G for Intraocular Injection because the vial label contains incorrect active and inactive ingredient information.
CooperSurgical is recalling 13 units of 2 MHz Waterproof OB probes because they were incorrectly labeled as 3 MHz probes.
United Orthopedic Corporation is recalling 14 U2 Total Knee System Tibial Inserts because the package contents did not match the product labeling.
Merit Medical Systems is recalling 8 dialysis kits containing misconfigured infant catheters. The 1-cuff catheters were incorrectly labeled as 2-cuff products.
Becton Dickinson is recalling specific Vacutainer tubes because they may cause underestimation of lead in blood samples when used with certain assays.
Centurion Medical Products Corporation is recalling Blood Draw Kits because the PVP Prep Pad does not meet required iodine levels for shelf life.
United Orthopedic Corporation is recalling 69 U2 Total Knee System Tibial Inserts because the package contents did not match the product labeling.
OMNIlife science Inc. is recalling 32 Apex Knee System Tibial Baseplates due to an incorrect expiration date on the external packaging.
Sunneen Health Foods is recalling 60 units of Vegan Buffalo Chicken Bites because the label fails to declare pecans.
3M is recalling specific ACE and Futuro ankle braces because they contain natural latex rubber but lack the required caution statement.
Zimmer Biomet is recalling 12 Humeral Stems because two lots were commingled and etched with incorrect lot numbers, creating a risk of using the wrong implant size.
Paige Common is recalling Almond Love Bar vegan chocolate bars due to undeclared soy lecithin. The product was distributed in Oregon.
Paige Common is recalling 46 packages of Maple Minis-Gluten Free Donut Bites sold in Oregon due to undeclared soy lecithin.
New Seasons Market LLC is recalling 45 units of 9-inch Asparagus and Goat Cheese Quiche because egg is missing from the 'Contains' statement on the label.
Ariola Foods is recalling Seviroli brand Cannoli Shells in New York due to undeclared soy lecithin.
Blue Moose of Boulder, LLC is recalling 504 units of All-Natural Ciolo Nut-Free Basil Pesto because the product contains undeclared tree nuts.
Cook Inc. is recalling 129,727 Amplatz Extra Stiff Wire Guides because the label fails to state that the product is heparin-coated.
American Pharmaceutical Ingredients LLC is recalling Oxytocin USP powder because stability data does not support the listed expiration dates.
Zimmer Biomet is recalling eight Vanguard CR Porous Femoral knee implants because they are labeled as 62.5mm Left Femurs but contain 70mm Right Femurs.
Cook Inc. is recalling 13 Central Venous Catheter Trays because the label fails to state that the product is heparin-coated.
Cook Inc. is recalling 45 Bentson Cerebral Wire Guides because the labels fail to state that the product is heparin-coated.