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.
Zimmer Biomet is recalling two ROSA BRAIN 3.0.0 devices in Ohio and Pennsylvania due to non-conforming product labels.
Resource Optimization & Innovation LLC is recalling 51 units of Regard Custom Surgical Packs because they contain a 3ml ChloraPrep With Tint unit with an incorrect label.
Leading Pharma, LLC is recalling Lorazepam tablets labeled as 0.5 mg but containing 1 mg. The recall addresses a labeling error affecting 2,952 bottles nationwide.
Zero Motorcycles is recalling 36 units of 2018 motorcycles because the Vehicle Emission Control Information label may display the wrong model year.
Gulf Stream Coach is recalling 2018 Geo and Breeze trailers because the Federal label incorrectly lists two axles instead of one, failing certification requirements.
Terumo BCT is recalling 281 bone marrow procedure packs because the patient labels contain incorrect lot numbers, catalog numbers, and expiration dates.
Karl Storz Endoscopy is recalling 496 boxes of High Flow Insufflation Tubing because some inner pouches are mislabeled with the wrong catalog number.
Terumo BCT is recalling specific bone marrow procedure packs because patient labels contain incorrect lot numbers, catalog numbers, and expiry dates.
Genzyme Corporation is recalling Clolar (clofarabine) injection vials because the package insert is incorrect or missing.
Arthrex is recalling 20 units of iBalance UKA knee implants due to incorrect part numbers and sizes printed on the patient label.
E & E Enterprises is recalling Muriel's Cheesey Bacon Dip because the label failed to declare milk and specific FD&C colors.
New American Food Products is recalling specific dark chocolate covered ginger products because they contain undeclared milk.
E & E Enterprises is recalling Muriel's Cheesey Pizza Dip because the label fails to declare milk and specific FD&C colors.
San Gennaro Foods is recalling sundried tomato polenta products because non-food-grade ink was printed directly on the packaging, allowing it to contact the food.
Northgate Technologies is recalling 186 electrohydraulic lithotripter probes due to incorrect reference numbers on labels, which could delay patient care.
San Gennaro Foods is recalling Ancient Harvest and Anna's Country Kitchen quinoa polenta because date coding ink was printed directly on the food contact surface of the packaging.
Becton Dickinson is recalling 90,000 blood collection tubes due to incorrect labeling at the case and shelf pack level.
bioMérieux is recalling VITEK2 GP-ID cards because atypical negative reactions caused quality control testing failures.
Ace Surgical Supply Co. is recalling 25 vials of Succinylcholine 20 mg/mL due to an incorrect expiration date on the outer poly bag labeling.
Aaren Scientific Inc. is recalling 786 boxes of AERO IOL Injection Systems because the recommended storage temperature on the label is incorrect.
Bioseal Corporation is recalling custom surgical kits containing Aplicare Providone Iodine Prep Pads due to incorrect expiration dates.
Dr. Reddy's is recalling Doan's Pain Relieving Cream because the lot number on the outer packaging does not match the bottle. This is a Class III labeling recall.
Forest River is recalling 2018 Prime Time Fury recreational trailers because the Federal Placard lists incorrect tire and rim sizes, which could lead to the installation of wrong replacement tires.
Earthbound Farm is recalling Asian Style Salad Kits because some contain dressing with undeclared egg and milk.
Great Lakes Cheese Co. is recalling American Accent Shredded Imitation Mozzarella Cheese because the label fails to identify whey and caseinate as milk ingredients.