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.
Giant Eagle is recalling Cheese Danish products containing undeclared egg. Consumers with egg allergies should not consume these items.
Giant Eagle is recalling Bolillo Rolls 6 Count because they contain undeclared egg. The product was sold in Maryland, Ohio, Pennsylvania, and West Virginia.
JCB Flavors is recalling Chili Powder Dark because it contains trace peanut allergens from a cumin ingredient.
Giant Eagle is recalling Heat/Serve Hot BBQ Boneless Chicken Wings with buffalo sauce due to undeclared milk. The product was sold in Maryland, Ohio, Pennsylvania, and West Virginia.
Giant Eagle is recalling Buffalo Boneless Chicken Wings because they contain undeclared milk, a major food allergen.
JCB Flavors is recalling specific Carne Asada seasonings because ground cumin used in the product tested positive for trace peanut allergens.
JCB Flavors is recalling Cherry Chipotle Wine Dip because the ground cumin ingredient tested positive for trace peanut allergens.
JCB Flavors is recalling various seasonings, including Milwaukee Firehouse Chili, because ground cumin used in the products tested positive for trace peanut allergens.
JCB Flavors is recalling Fajita Seasoning because it contains ground cumin that tested positive for trace peanut allergens.
Hope Foods is voluntarily recalling one lot of Kale Pesto Hummus because it contains undeclared walnuts. Consumers should check for the specific lot code and UPC.
JCB Flavors is recalling Andouille Sausage because ground cumin used in the product tested positive for trace peanut allergens.
Beckman Coulter is recalling MicroScan Dried Gram Negative MIC/Combo Panels because a technical bulletin failed to mention performance limitations for Proteus mirabilis and Imipenem.
Supervalu is recalling Essential Everyday Chocolate Covered Peanuts because the product may contain undeclared raisins. The recall affects 43 cases distributed in several US states.
Bard Access Systems is recalling 700 units of the PowerLoc MAX Safety Winged Infusion Set due to a potential incorrect Maximum Flow rate label on the packaging.
Fresenius Medical Care is recalling 2008 Series Hemodialysis Machines because the Acetate value for GranuFlo is displayed incorrectly on the Select Concentrate screen.
Fresenius Medical Care is recalling 2008T hemodialysis machines because the Select Concentrate screen incorrectly displays the GranuFlo acetate value as 4mEq/l instead of 8mEq/l.
Alphatec Spine is recalling 14mm Trestle Luxe screws that were incorrectly labeled and laser-marked as 14mm but are actually 16mm.
Beckman Coulter is recalling MicroScan Microbiology Systems panels because a 2013 bulletin failed to mention a performance limitation for Proteus mirabilis and Imipenem.
Beckman Coulter is recalling MicroScan Dried Gram Negative MIC/Combo Panels because a technical bulletin omitted a performance limitation for Proteus mirabilis.
Integra LifeSciences is recalling 90 Tuohy needles that were incorrectly labeled as 5 inches when they are actually 3.5 inches.
Iberia Foods Corp. is recalling IBERIA Yellow Rice Spanish Style Enriched Parboiled Rice due to an unintended ingredient change and unpleasant taste and smell.
Beckman Coulter is recalling MicroScan Dried Gram Negative MIC/Combo Panels because a technical bulletin failed to mention performance limitations for Proteus mirabilis and Imipenem.
Beckman Coulter is recalling MicroScan Dried Gram Negative MIC/Combo Panels because a technical bulletin failed to mention performance limitations for Proteus mirabilis.
Coloplast is recalling 11 units of the 9.5 mm Genesis Malleable Penile Prosthesis because the retail box and patient labels incorrectly state the size as 9 mm.
Beckman Coulter is recalling MicroScan Dried Gram Negative MIC/Combo Panels because a technical bulletin omitted a performance limitation for Proteus mirabilis.