Hazard
9,622 recalls in our database tag this hazard, drawn from FDA, USDA FSIS, CPSC, and NHTSA source notices.
Of the 9,622 mis labeling recalls we have scored against our rubric, 163 (2%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 590 (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.
Dr. Reddy's Laboratories is recalling Tizanidine Tablets because bottle labels may be missing the product strength and other printing details.
Southeast Toyota is recalling specific 2008-2013 models because weight labels were inaccurate, potentially leading to vehicle overloading and tire failure.
Wholesale Baking, Inc. is recalling Ruthies Cashew Raisin Breakfast Cookies because butter and half & half are listed, but milk is not declared on the label.
Miravalle Food, Inc. is recalling Pan Rallado Sazonado seasoned bread crumbs due to undeclared wheat and missing nutritional facts.
Biomerieux Inc is recalling VITEK 2 60 computer systems due to a potential error that could link test results to the wrong patient.
Biomerieux Inc. is recalling VITEK 2 Compact computer systems because a software issue could link test results to the wrong patient.
Biomerieux Inc. is recalling VITEK 2 XL computer systems equipped with specific Hewlett-Packard PCs due to a potential risk of linking test results to the wrong patient.
Cooper Surgical is recalling 80 Omniflex Diaphragms because the incorrect size was printed on the outer packaging.
Synthes USA HQ, Inc. is recalling 148 Dens Instrument Sets because there are no screws specifically indicated for the procedure.
CareFusion 213, LLC is recalling 698,000 SEPP 70% Isopropanol applicators because the product is not sterile, making the labeling misleading regarding sterility claims.
CareFusion is recalling SEPP 10% Povidone Iodine Solution applicators because the product is not sterile, making the sterility claims on the label misleading.
Biomerieux Inc is recalling VITEK 2 AST-ST01 Streptococcus Susceptibility Cards because the package insert did not list the correct limitations of use and performance requirements.
CareFusion is recalling Blood Culture Prep Kit II units because the product is not sterile, making the labeling misleading regarding sterility claims.
CareFusion 213, LLC is recalling 46,500 Donor Prep Kits because the labeling is misleading regarding sterility claims. The product is not sterile.
CareFusion 213, LLC is recalling 544,500 FREPP/SEPP kits because the product is not sterile, but the labeling misleadingly implies it is.
CareFusion 213, LLC is recalling SEPP 2% Iodine Tincture applicators because the product is not sterile, making the labeling misleading regarding sterility claims.
Servatii Inc is recalling 90 one-pound packages of Banana Nut Bread because the ingredient list incorrectly identifies walnuts instead of pecans.
Cooper Surgical is recalling 45 units of Incontinence Dish pessaries because the outer package may not reflect the actual product size.
Cooper Surgical is recalling Gellhorn Flexible Pessaries because the outer packaging may not reflect the actual size of the device inside.
Kettle Foods is recalling Honey Roast Nuts and Fruit Trail Mix because it was made with dried pineapple containing sulfur dioxide instead of untreated pineapple.
Cooper Surgical is recalling 31 units of Incontinence Dish Folding Pessaries because the outer packaging may not reflect the actual product size.
Cooper Surgical is recalling 70 units of Cube Pessaries because the outer packaging may not reflect the actual size of the product inside.
CareFusion is recalling Sepp Compound Benzoin Tincture products because labeling incorrectly implies the antiseptic solution is sterile, when only the applicator is sterile.
Cooper Surgical is recalling Gellhorn Flexible Pessaries because the outer packaging may not accurately reflect the size of the product inside.
Ultradent Products, Inc. is recalling 104 units of Opalescence Treswhite Supreme Peach Patient Kits due to incorrect shelf-life labeling.