Hazard
9,611 recalls in our database tag this hazard, drawn from FDA, USDA FSIS, CPSC, and NHTSA source notices.
Of the 9,611 mis labeling recalls we have scored against our rubric, 161 (2%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 589 (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.
Dayton Nut Specialties Inc is recalling Creation Special Snack Mix because the packaging failed to declare peanuts, tree nuts, soy, wheat, and Yellow #5.
Biomet, Inc. is recalling specific lots of Intramedullary Bone Saw Cam Assemblies because they were incorrectly labeled as Saw Blade Assemblies.
China Daheng Group Inc. is recalling 238 Denlase and Penlase dental laser systems because the user manuals lacked required calibration procedures.
Stryker is voluntarily recalling 90 units of 2.5MM Aggressive Sinuscopic Shaver Blades because the etched line guide is missing the required 1cm to 7cm number scale.
Ortho-Clinical Diagnostics is recalling VITROS White Correction Factor Slides because an incorrect assay value was printed on the carton, which may delay reporting of specific test results.
Biomet is recalling 10 Intramedullary Bone Saw Cam Assemblies because they were incorrectly labeled as Saw Blade Assemblies.
Biomet, Inc. is recalling specific lots of the Intramedullary Bone Saw CAM Assembly because the Saw Blade Assembly was incorrectly identified as a CAM Assembly.
Biomet 3i, LLC is recalling 704 units of Endobon Xenograft Granules 0.5 ML because individual pieces may have incorrect labels with the wrong batch number.
Meijer Distribution is recalling Pretzel Hamburger Buns and Pretzel Demi Rolls because the whey powder ingredient is not identified as milk in the allergen statement.
C. H. Guenther & Sons, Inc. is recalling Morrison's Brown Gravy Mix mislabeled as pancake mix due to undeclared soy.
Meijer Distribution is recalling Pretzel Dinner Rolls because milk is not listed as an allergen. People with milk allergies risk serious reactions.
Raymond-Hadley Corp. is recalling StoneWall Kitchen Chocolate Coconut Cupcake Mix because the packaging fails to list milk as an allergen, despite containing sodium caseinate.
Savory Foods, Inc. is recalling Mary Ann's Chocolates Signature Assortments because the ingredient panels failed to list peanuts, specific tree nuts, soy, and certain food dyes.
Nissan is recalling 2014 Infiniti QX80 vehicles because the certification label lists an incorrect Gross Axle Weight Rating, potentially allowing vehicle overload.
F & S Produce Co., Inc. is recalling Roasting Cinnamon Butternut Squash because the product is mislabeled. The recall covers 429 units distributed in California.
Leica Biosystems is recalling 78 units of the ScanScope System software to clarify usage with specific RUO products.
Fougera Pharmaceuticals is recalling 493,192 tubes of Triamcinolone Acetonide Cream 0.1% because the end flap incorrectly displays 01% instead of 0.1%.
Steris is recalling VERIFY SixCess 270FP Challenge Packs because the outer shipping package for one lot incorrectly identifies the lot number.
Pinnacle Biologics is recalling 261 vials of Photofrin (porfimer sodium) because the printed expiration date is incorrect.
Jaguar is recalling 2013 XJ and XF vehicles because they lack required certification labels specifying weight ratings. This non-compliance could lead to vehicle overloading and increased crash risk.
Rise'n Roll Bakery is recalling Bavarian Creme Donuts because they contain an undeclared egg ingredient, posing a risk to individuals with egg allergies.
Rise'n Roll Bakery is recalling Caramel Donuts because they contain egg, which is not listed on the label. Consumers with egg allergies should not eat the product.
Rise'n Roll Bakery is recalling chocolate donuts because they contain undeclared egg, a major food allergen.
Rise'n Roll Bakery is recalling Cinnamon Caramel Donuts and Donut Holes because they contain an undeclared egg ingredient. The products were sold in multiple states and online.
Rise'n Roll Bakery is recalling White Powdered Donuts because they contain an undeclared egg ingredient, posing a risk to consumers with egg allergies.