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.
Siemens Healthcare Diagnostics is recalling IMMULITE Gastrin assays because biotin interference is not listed in the instructions for use.
Bard Peripheral Vascular Inc is recalling 181 POWERPORT ClearVUE Slim catheters because the included Patient ID Card has incorrect flushing instructions.
Siemens is recalling Dimension Free Thyroxine reagent cartridges because the instructions for use incorrectly state the level at which biotin does not interfere.
Hyphen BioMed is recalling ZYMUTEST HIA MonoStria kits because the package insert incorrectly lists serum and other fluids as valid sample types.
Siemens Healthcare Diagnostics is recalling EMIT II Plus 6-Acetyl Morphine reagents due to incorrect calibrator levels listed in the calibration steps.
MHC Medical Products LLC is recalling 46,600 EasyTouch insulin syringes because retail shelf cartons may display an incorrect lot number.
Siemens Healthcare Diagnostics is recalling Syva EMIT II Plus 6-Acetylmorphine reagents because the calibrator level listed in the qualitative calibration steps is incorrect.
Ford is recalling 2018 Ecosport vehicles because they have European brake cap labels and manuals, which may confuse owners and affect brake performance.
Mccall Farms is recalling Happy Harvest Leaf Spinach cans because they may contain boiled peanuts instead of spinach. The recall affects 739 cases distributed across 16 states.
Independent Nutrition, Inc. is recalling Ignite High Endurance Pre-Workout Supplement because the label declares whey protein but fails to declare milk.
Independent Nutrition, Inc. is recalling Ignite High Endurance Pre-Workout Supplement Vanilla because the label declared whey protein but failed to declare milk.
Southwest Technologies Inc. is recalling hypothermia mitts, slippers, and caps because they are misbranded for chemotherapy use and linked to two frostbite events.
Wysong Corporation is voluntarily recalling Protein Key brand protein meals due to undeclared soy. Consumers with soy allergies should not consume the product.
Independent Nutrition, Inc. is recalling Ignite High Endurance Pre-Workout Supplement because the label declared whey protein but failed to declare milk.
Independent Nutrition, Inc. is recalling Ignite High Endurance Pre-Workout Supplement because the label declares whey protein but fails to declare milk.
Stuffed Foods LLC is recalling Edamame Burgers because they contain undeclared wheat, posing a risk to individuals with wheat allergies or celiac disease.
Southwest Technologies is recalling hypothermia caps and other products misbranded for chemotherapy use, following reports of frostbite.
Independent Nutrition, Inc. is recalling Enduravol Elite Pre-Workout because the label declared whey protein but failed to declare milk, a major allergen.
Wysong Corporation is voluntarily recalling Protein Key brand protein meals due to undeclared soy. Consumers should stop using the product.
Beijing Syntech Laser Co., Ltd is recalling 92 UL C02 Laser surgical lasers because the required certification label was not affixed to the product.
Beijing Syntech Laser Co., Ltd is recalling 38 Trixel C02 Laser surgical lasers because the required certification label was not affixed to the product.
Beijing Syntech Laser Co., Ltd is recalling 11 APOLLO V+ Medical Platform surgical lasers because the required certification label was not affixed to the product.
Teleflex Medical is recalling 25 units of the LMA MADgic device due to missing or incomplete information on the package label.
Stryker is recalling three 6381 M-1 Cot Fasteners because their manuals contain incorrect information and missing warnings.
Beijing Syntech Laser is recalling six APOLLO JV+ Medical Platform surgical lasers because the required certification label was not affixed to the products.