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.
Zingerman's Bakehouse is recalling Cape Cod Cranberry Walnut Pies because labels failed to identify milk and wheat as ingredients.
Zingerman's Bakehouse is recalling Nueske's Bacon Apple Coffeecake because labels failed to identify milk, wheat, and soy allergens.
HP Hood LLC is recalling Blue Diamond Almond Breeze Almond Milk because it may contain undeclared cocoa and evaporated cane juice.
Ferring Pharmaceuticals is recalling Novarel (Chorionic Gonadotropin) vials because the package insert is missing a warning about anaphylaxis.
Stryker Howmedica Osteonics Corp. is recalling 7 units of non-sterile Femoral Offset Bushing Triathlon Revision Instruments due to incorrect or missing rotational markings.
Stryker Howmedica Osteonics is recalling 8 Tibial Offset Bushings because rotational reference numbers were marked incorrectly or missing.
CSM Bakery Products NA is recalling Murray's Waffle Cone Dip due to undeclared milk and soybean oil allergens caused by mislabeling.
Chicken of the Sea is recalling Solid White Tuna in Water because the label fails to declare soy, a major food allergen.
Hillshire Brands is recalling Jimmy Dean French Toast & Sausage Sandwiches because the back label lists ingredients for a different product, omitting egg and soy.
Quality Dairy Farms Inc. is recalling Mercer's Ice Cream Cookies 'N Cream because the product contains soy lecithin but the label only lists lecithin.
Quality Dairy Farms Inc. is recalling Mercer's Ice Cream Cream N' Coffee Fudge because the product contains soy lecithin, which was not explicitly listed on the ingredient statement.
Quality Dairy Farms Inc. is recalling Mercer's Ice Cream Old Fashioned Cookie Dough because the product contains soy lecithin, which was not explicitly listed on the ingredient statement.
Metrex Research is recalling Pinnacle Cure Sleeves because boxes labeled for 11mm light guides contain sleeves for 7mm or 8mm guides.
Biomet, Inc. is recalling four Echo Bi-Metric hip stems because the etching on the 11mm stems incorrectly indicated they were 13mm stems.
Procter & Gamble is recalling 17,532 bottles of Vicks NyQuil Cold & Flu because portions of the dosing directions and warnings are obscured.
Diamedix Corporation is recalling 65 Is-anti-Sm Test Kits because the positive control recovered high out of specification.
Chrysler is recalling 2013 Dodge Durango vehicles with incorrect seating capacity labels that may overstate capacity, potentially increasing injury risk in a crash.
Biomerieux Inc is recalling 0.9% Sodium Chloride Injections that were distributed as 0.45% Sodium Chloride Saline bags for use with the VITEK 2 system.
Biomerieux Inc is recalling 22 B.40 software updates because a defect may cause patient information to be mislabeled on culture specimen bottles.
BioMerieux is recalling 23 B.40 software update kits because a software miscommunication may cause patient information to be mislabeled on culture specimen bottles.
BioMérieux is recalling 860 units of 3D B.40 software updates due to a defect that may mislabel patient information on culture specimen bottles.
BioMerieux is recalling 620 units of 3D B.40 software updates because a software error may mislabel patient information on culture specimen bottles.
BioMerieux is recalling BacT/ALERT Control Modules because a software issue may cause patient information to be mislabeled on culture specimen bottles.
BioMerieux is recalling B.40 software updates because a defect may cause patient information to be mislabeled on culture specimen bottles.
BioMérieux is recalling BTA3D Control software due to a defect that may mislabel patient information on culture specimen bottles.