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.
CIVCO Medical Instruments is recalling 297 boxes of SonoSite Needle Guide Brackets because some units lack required product labeling.
Angiodynamics Inc. is recalling specific lots of BioFlo PICCs labeled with incorrect expiration dates that extend shelf life beyond validated testing.
First Source, LLC is recalling Chocolate and Nut Trays because they contain undeclared pecans and cashews. The product was distributed in six states.
English Bay Batter L.P. is recalling Schnucks BIG & FLAKY CRESCENT ROLLS due to undeclared milk in the ingredient list and contains statement.
Tillamook is recalling Vanilla Chocolate Chip ice cream because it contains undeclared color additives Amaranth and Yellow No. 6.
Frutarom USA Inc. is recalling 1,018 bottles of Sebastiano's French Vanilla syrup because the product contains sugar despite being labeled 'Naturally Sugar Free.'
NOW Foods is voluntarily recalling 61 bottles of Vitamin B-50 Complex with C 100 Veg Caps because they are mislabeled as Vitamin B-50 mg 100 Veg Caps.
Tosoh Bioscience is recalling 1,228 AIA-360 Analyzers to update labeling and training materials regarding maintenance and reagent requirements.
Fresenius Kabi is recalling 1,312,350 vials of Sodium Chloride Injection because labels incorrectly state the stoppers do not contain natural rubber latex.
Fresenius Kabi is recalling 23.7 million sodium chloride vials because labels incorrectly state the stoppers do not contain natural rubber latex.
Helena Laboratories is recalling 43 Gel Alkaline Phosphatase Isoenzyme Control Kits due to customer complaints of lower enzyme activity.
Neomed Inc is recalling NeoConnect Enteral Extension Sets because the sterile pouch labels display an incorrect expiration date of 2016-11-19 instead of 2019-11-09.
3-D Meats, LLC is recalling approximately 47 pounds of ready-to-eat beef snack sticks because they are misbranded and may contain undeclared milk, a known allergen.
Amboy Group, LLC is recalling raw boneless and skinless poultry products because they are misbranded and may contain undeclared milk, egg, and soy.
Chukar Cherry Company is recalling 569 pouches of Ultra Dark Chocolate Cocoa Pecans because the product contains milk, which is not listed on the label.
Chukar Cherry Company is recalling 502 pouches of Organic Ultra Dark Vanilla Chocolate Rainier Cherries because the product contains milk, which is not listed on the label.
Shirleys Cookie Company is recalling Chocolate Peanut Butter Whoopie Pies labeled as Chocolate Whoopie Pies because the peanut allergen is not declared on the packaging.
La Casa del Limber, Inc. is recalling Oreo Limber because the label failed to declare wheat as an ingredient.
Chukar Cherry Company is recalling Ultra Dark Chocolate Amaretto Rainier Cherries because the product contains milk, which is not listed on the label.
Chukar Cherry Company is recalling Organic Ultra Dark Orange Chocolate Tart Cherries because the product contains milk, which is not listed on the label.
Nor Cal Food Solutions LLC is recalling Purveyors Kitchen Pumpkin Pesto Tapenade because the product does not declare walnuts as an ingredient or allergen.
Chicago Importing Co is recalling Finax Muesli with 45% Fruit because the ingredients statement does not indicate the presence of coconut.
Thatchers is recalling 2,898 units of 8-ounce Gingerbread Popcorn sold at Disney locations because the ingredient list declares flour but fails to declare wheat.
Siemens is recalling Dimension Vista Lactate Dehydrogenase reagent cartridges because they may produce falsely elevated results if used after Lactic Acid assays.
Elaboraciones Felo, Inc. is recalling Pizza Turnovers because the products failed to declare wheat and soy allergens. The recall covers 7,011 cases distributed in Puerto Rico.