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.
AMD Medicom Inc. is recalling Level 2 masks that may have been packed in Level 3 boxes, creating a risk of using lower-protection masks.
AMD Medicom is recalling Level 3 masks because Level 2 masks may have been packed in Level 3 boxes. The masks are visually indistinguishable, creating a risk of using lower protection.
Becton Dickinson is recalling BD Posiflush syringes because a limited number of experimental units were mixed with standard products.
Becton Dickinson is recalling BD Posiflush Pre-Filled Normal Saline Syringes because a limited number of experimental units were mixed with standard stock.
Nucryo Vascular Inc. is recalling 49 PolarCath Balloon Catheters because they were mislabeled as ethylene oxide sterilized instead of E-beam sterilized.
Cincinnati Sub-Zero is recalling 3,932 Blanketrol III Hyper-Hypothermia Systems to add warnings about tissue damage from extended high temperatures and clarify automatic mode usage.
Angiodynamics Inc. is recalling 30 Starburst Talon Semi-Flex Electrosurgical Devices that were incorrectly labelled as Starburst MRI Semi-Flex devices, potentially causing procedural delays.
Centurion Medical Products is recalling 525 Epistaxis Tray Kits because they contain major nasal decongestant spray.
Randox Laboratories is removing N-proBNP claims from Liquid Cardiac Controls due to decreased recovery in recent lots.
Randox Laboratories is recalling Liquid Cardiac Controls (CQ5051) to remove N-proBNP claims due to decreased recovery in recent lots.
Randox Laboratories is recalling Liquid Cardiac Controls (CQ5053) to remove N-proBNP claims due to decreased recovery in recent lots.
Hager & Meisinger is recalling 2,500 dental carbide burs because a 1.0 mm blade may have been packaged in 0.9 mm packaging.
X-Gen Pharmaceuticals is recalling Levetiracetam Injection vials because the incorrect package insert version was attached to the product.
Deck Source is recalling Cutek Proclean Professional Wood Restoration because its label violates Federal Hazardous Substance Act requirements, posing a risk of poisoning.
Harris Teeter Supermarkets is recalling Mint Chocolate Chip Ice Cream because the ingredient soy was not declared in the product's ingredient statement or allergen declaration.
Harris Teeter is recalling specific containers of Smooth & Creamy Take the Cake Ice Cream because the ingredient soy was not declared on the label.
Harris Teeter is recalling Mint Chip Old Fashioned Ice Cream because soy was not declared in the ingredient statement or allergen declaration.
Gilster-Mary Lee Corp. is recalling Food Lion Creamy Chocolate Frosting because cream cheese frosting was mislabeled as chocolate, failing to declare the major allergen milk.
Implant Direct is recalling 23 dental implants because a QA inspection found a healing collar was packaged instead of the implant.
Daimler Trucks North America is recalling 2020 Freightliner Econic SD vehicles because certification labels contain incorrect gross axle weight rating information, which may lead to axle overloading.
BrucePac is recalling ready-to-eat chicken sausage products because they contain an undeclared pork casing. No adverse reactions have been reported.
Arcimoto is recalling 2019 FUV motorcycles because the ignition switch lacks required 'Ignition' and 'Off' labels, which could lead to operator error.
Fisherman's Pride Processor is recalling 1,872 units of Schwan's Garlic Herb Shrimp due to undeclared milk and soy lecithin.
Creative Food Processing is recalling raw chicken skewers because they contain wheat, a known allergen, that is not declared on the label.
Randox Laboratories is recalling 17 Rheumatoid Factor Standard kits because assigned values over-recovered against reference material. The values have been adjusted to align with the reference standard.