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.
Nutreglo Products, LLC. is recalling Blood & Internal Cleanser dietary supplements because laboratory results showed incorrect iron levels and drug claims.
Absonutrix is recalling Lyfetrition Vitamin B12 supplements because the product did not contain the vitamin listed on the label.
Nutreglo Products, LLC. is recalling two dietary supplements due to incorrect ingredient amounts and undeclared drug claims.
Nueske's Meat Products is recalling approximately 12,946 pounds of braised pork products because they may contain undeclared brown rice flour and glycerin.
L&D Market Inc. is recalling wasabi chicken wraps due to misbranding and undeclared milk allergens. The products were shipped to retail locations in Cambridge, Massachusetts.
World Variety Produce Inc. is recalling Melissa's Spicy Edamame because the included flavoring packet contains oyster sauce, an undeclared allergen.
Smith & Nephew is recalling two Birmingham Hip Resurfacing Femoral Heads because they were distributed in the US with non-US labeling.
Stryker GmbH is recalling Farabeuf Clamps for 3.5mm Screws PRO because laser etching indicating compression or distraction mode is on the wrong side of the lever arm.
Smith & Nephew is recalling six Birmingham Hip Resurfacing Acetabular Cups because they were distributed in the US with international labeling instead of FDA-approved instructions.
Quantimetrix Corporation is recalling 20 kits of Dropper Plus Point-of-Care Urinalysis Dipstick Control because they contained an incorrect lot of Level 1 vials.
Keystone is recalling 2019 Summerland recreational trailers because the Federal Identification Label lists an incorrect tire rim size, which could lead to improper rim replacement.
Land O'Frost is recalling 4,944 pounds of Black Forest Ham because the back of the package incorrectly identifies the product as Honey Smoked Turkey Breast.
Allergan is recalling Taytulla softgel capsules because the tablets are out of sequence. This affects 168,768 blister cards distributed nationwide.
Roche Diabetes Care is recalling Accu-Chek Inform II test strips because they may produce errors or biased results, potentially leading to incorrect user actions.
Shearers Foods is recalling Meijer Dill Pickle Flavored Classic Crunch Potato Chips because milk was not declared on the label.
Siemens Healthcare Diagnostics is recalling specific lots of Dimension Gentamicin Flex reagent cartridges because they may produce inaccurate test results at the low end of the measurement range.
Zimmer Biomet is recalling 16 units of 75mm tibial tray implants that may be incorrectly labeled as 79mm. This error could lead to surgical delays or the need for immediate revision surgery.
Divvies LLC is recalling 447 Semi-Sweet Peppermint Bars sold nationwide online because the product may contain traces of milk.
Keystone Dental Inc is recalling 72 Prima Plus dental implants due to mislabeling. The devices were distributed to dental professionals in 14 US states.
Honda is recalling 2018 Civic vehicles because random characters on the certification label may prevent owners from verifying safety recall eligibility.
Philips is recalling IntelliVue MX40 Patient Monitors because five warning statements are missing from the instructions for use.
Philips is recalling 94 IntelliVue MX40 Patient Monitors because five warning statements are missing from the instructions for use.
Yukon Jackson is recalling Herd of Turtles milk chocolate because pecans are listed in the ingredients but missing from the 'Contains' statement.
Yukon Jackson is recalling Herd of Turtles dark chocolate because pecans are listed in ingredients but not in the 'Contains' statement.
Yukon Jackson is recalling Coffee Toffee because pecans are listed in the ingredients but not in the 'Contains' statement.