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.
Jaguar is recalling 1,346 model year 2015 XJ vehicles because the owner's manual incorrectly describes the Occupant Sensor System, potentially increasing injury risk in a crash.
BMW is recalling 2014-2015 MINI Cooper Hardtop vehicles because the Tire Information Placard lists an incorrect maximum capacity weight, failing to comply with federal safety standards.
Primecut Meats is recalling approximately 17,700 pounds of chicken breast fritters because the products contain eggs, a known allergen, that are not declared on the label.
Siemens is recalling 7 ADVIA Chemistry XPT systems in Washington due to a software defect that may cause critical results to be overwritten.
CR Brands is recalling Mean Green cleaner and degreaser products because they may contain ammonia despite labels stating otherwise, posing a chemical hazard.
NatureBox, Inc. is recalling Sweet Blueberry Almonds because the product label failed to list soy lecithin, an ingredient included in the recipe.
Biocare Medical is recalling three lots of MUM-1 antibody because staining intensity drops over time, potentially affecting diagnostic accuracy.
SCA Pharmaceuticals is recalling 972 syringes of Glycopyrrolate injection distributed in Louisiana because a printing error made the expiration date appear incorrect.
Mentor Texas, LP. is recalling 45 units of MENTOR MemoryGel Resterilizable Gel Sizers because they contain incorrect instructions for use.
Abdallah Candies is recalling Holiday Caramel Bites because a customer found a peanut butter bite in the package.
Taylor Farms Pacific is recalling Citizen Chef Organic Superfood Salad due to undeclared milk on individual units. The outer packaging is labeled correctly.
Exactech, Inc. is voluntarily recalling 96 Optetrak femoral implants due to mislabeling. The devices were distributed internationally to 13 countries.
Spinal Elements is recalling Ti-Bond marketing literature because the content regarding the Ti-Bond coating is unsubstantiated and misleading for spine applications.
US Foods is recalling approximately 700 pounds of beef fajita strips because the product contains undeclared peanuts, a known allergen.
Shirks Meats is recalling approximately 1,062 pounds of smoked pork andouille sausage because it contains undeclared peanuts. No adverse reactions have been reported.
Ev3, Inc. is recalling two lots of Protege Rx Tapered Carotid Stent Systems due to a product labeling error. The affected units were distributed internationally.
Ev3, Inc. is recalling two lots of Protege Rx Tapered Carotid Stent Systems due to a product labeling error. The affected devices were distributed internationally.
Jaymac Pharmaceuticals is recalling J-TAN D PD Drops because the product is labeled 'Dye Free' but contains Red Dye 40.
B. Robert's Foods is recalling approximately 4,474 pounds of chicken noodle soup because it was mislabeled as chicken and wild rice soup, failing to declare the egg allergen.
Horiba Instruments is recalling Lite DM software versions 2.0.0.19 and lower due to a bug that may apply test results to the wrong patient order.
The Kroger Co is recalling Private Selection Extreme Moose Tracks Ice Cream because it may contain peanuts not listed on the label.
Willy's Inc is recalling 1,944 containers of Just Peachy Salsa because the label failed to list FD & C Yellow #5, a food color additive.
Intuitive Surgical is recalling Fluorescence Imaging Procedure Kits because storage conditions for indocyanine green are missing from the packaging.
Unistrip Technologies LLC is recalling 7,175 units of UniStrip1 Blood Glucose Test Strips because the company failed to submit a 510(k) for device labeling changes.
LNK International recalled specific lots of Walgreens Aspirin Free Tension Headache Caplets because they contain sucralose, an ingredient not listed on the label.