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.
Integra LifeSciences Corp. is recalling 39 units of the UNI-CP System due to incorrect labeling on the plate.
Forest River is recalling 2017 Cherokee recreational trailers because the Federal Placard lists incorrect tire and rim sizes, which may lead to installing wrong replacement tires.
Chip'n Dipped is recalling Dark Almond 63% Cacao chocolate bars because they contain undeclared milk. The product was sold in New York, Pennsylvania, and Massachusetts.
Bell Stone Toffee is voluntarily recalling White Chocolate Toffee because the label declared butter but failed to identify the presence of the milk allergen.
Bell Stone Toffee is voluntarily recalling Toffee Chocolate Bars because the packaging failed to identify milk as an allergen, despite listing butter as an ingredient.
Synthes (USA) Products LLC is recalling two PRODISC Orthopedic Manual Surgical Instrument struts used in spinal surgery because they are incorrectly etched and labeled with the wrong size.
Bell Stone Toffee is voluntarily recalling specific lots of toffee products because the labels failed to identify milk as an ingredient, despite declaring butter.
World Organic Corp. is recalling Theravits 100 and The Supreme One vitamins because the labels incorrectly state they contain no common allergens while containing fish liver oil.
Matrix Surgical Holdings is recalling 28 mandible onlay implants due to packaging mislabeling where left-sided packaging contained right-sided devices.
Medtronic is recalling 22,298 SynchroMed II software application cards to update the priming bolus function and pump labeling.
Forest River is recalling 2017 Prime Time Crusader recreational trailers because the Federal placard incorrectly lists axle capacity as 7,000 lbs instead of 6,000 lbs, which could lead to overloading.
Rochester Meat Company is recalling approximately 13,330 pounds of pork sausage products because they contain undeclared monosodium glutamate (MSG). The products were shipped to institutional locations in five states.
Volkswagen is recalling 2017 Beetle and Jetta GLI vehicles because incorrect tire information labels may cause operators to overload the vehicle, increasing crash risk.
Volkswagen is recalling 2017 Jetta vehicles because incorrect tire information labels may lead to vehicle overloading, increasing crash risk.
Athens Baking Company is recalling specific lots of Trader Joe's Harvest Whole Wheat Bread because they fail to declare cultured whey or list milk as an allergen.
Falafel King is recalling 1,380 containers of Tzatziki Sauce due to undeclared milk on the label. The product was distributed in Colorado, New Mexico, Utah, and Nebraska.
Vascular Solutions is recalling 633 units of GrebSet Micro-Introducer Kits because the guidewires have a shorter shelf life than the kit expiration date.
Smith & Nephew is recalling 2,646 Dyonics Saw Blades because they are provided sterile but lack an expiration date on the label.
Smith & Nephew is recalling 8,748 Dyonics Saw Blades because the single-use sterile devices lack expiration dates on their labels.
Penn Herb Company is recalling Nature's Wonderland Sinus & Lung Care capsules because Ginkgo Leaves were accidentally added to the herbal blend instead of Ginger Root.
Smith & Nephew is recalling 4,500 Dyonics Saw Blades, Short (Product Number 3703) because the single-use sterile devices lack expiration dates on their labels.
Sandoz Inc. is recalling Transderm Scop patches because the outer carton contains incorrect instructions for cutting the patch.
Smith & Nephew is recalling 3,462 Dyonics Saw Blades, Narrow (Product Number 3705) because the single-use sterile devices lack an expiration date on the label.
Smith & Nephew is recalling 1,410 Dyonics Saw Blades because the single-use sterile devices lack expiration dates on the label.
Reckitt Benckiser LLC is recalling Durex Pleasure Pack condoms because the package labeling is missing information about the active ingredient Benzocaine.