Hazard
9,606 recalls in our database tag this hazard, drawn from FDA, USDA FSIS, CPSC, and NHTSA source notices.
Of the 9,606 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.
Shaman Botanicals, LLC is recalling White Vein Advanced Alkaloids Chewable Tablets because testing found the active ingredient 7-hydroxymitragynine is present in a quantity greater than the labeled specification.
Fayus Inc. is voluntarily recalling OLA-OLA Pounded Yam (Iyan) IYANINSTANT in multiple sizes due to undeclared milk. The product was distributed in six US states and two foreign countries.
Prince Bakery Inc is recalling 150 units of Prince Sesame French Bread in New York because sesame is not declared in the ingredient statement.
Prince Bakery Inc is recalling 150 units of Pan De Manteca in New York because milk is not declared in the Contains statement.
Prince Bakery Inc is recalling 150 units of Prince Italian Bread in New York because sesame is not declared in the ingredient statement.
Prince Bakery Inc is recalling 150 units of Italian and French bread in New York because sesame is not declared in the ingredient statement.
Wonton Specialist is recalling 700 bags of cooked noodles in New York, New Jersey, and Pennsylvania due to undeclared FD&C Red No. 40.
Allies Group Inc. is recalling 27,492 sachets of THE ONE SPF 50 Invisible Sunscreen Gel because firm testing indicated the product may not reliably provide the stated SPF 50 protection.
Wonton Specialists is recalling 16 oz wonton skins sold in NY, NJ, and PA due to undeclared FD&C Red No. 40.
Wonton Specialist Inc. is recalling 16 oz bags of Dumpling Skin due to undeclared FD&C Red No. 40. The product was distributed in New York, New Jersey, and Pennsylvania.
B Braun Medical Inc is recalling specific lots of Discofix Four Way Stopcock Extension Sets because the carton shipper labels display an incorrect expiration date.
Wonton Specialist Inc. is recalling Pan Fried Noodles due to undeclared FD&C Red No. 40. The product was distributed in New York, New Jersey, and Pennsylvania.
Jaime's Foods ATX, LLC is recalling Jalapeno Ranch in 16 oz. glass jars because the product contains an undeclared egg allergen. The recall affects 102 cases distributed in Texas.
Sun Noodle is recalling Sura Tanmen Hot and Sour Flavor ramen kits because the soup packet contains fish but the label does not declare it.
Toyota is recalling specific 2024-2026 models because inaccurate load capacity labels may lead to vehicle overloading and increased crash risk.
AVID Medical is recalling 45 Halyard DAVINCI TRUCUSTOM Foley catheter kits because the labeling fails to identify that the statlock component contains natural rubber latex.
Byron White Formulas is recalling its A-FNG Herbal Supplement because the label fails to declare walnuts in English, posing a risk to consumers with nut allergies.
Byron White Formulas is recalling A-L Complex Herbal Supplement because the label does not declare walnuts in English, posing a risk to individuals with nut allergies.
Byron White Formulas is recalling its A-P Herbal Supplement because the label fails to declare walnuts in English, posing a risk to individuals with nut allergies.
Medline is recalling 45 Trach Tube Kits (SKU DYKM2330) due to a component labeling discrepancy. The recall covers units distributed in California.
AVID Medical is recalling 63 Halyard Total Joint kits because the labeling fails to identify that the statlock component contains natural rubber latex.
AVID Medical, Inc. is recalling 130 Halyard Total Joint kits because the labeling fails to identify that the statlock component contains natural rubber latex.
AVID Medical is recalling 78 Halyard Total Joint kits because the labeling fails to identify that the statlock component contains natural rubber latex.
Henry Schein Inc. is recalling specific lots of Structur 2 SC Temporary Resin Cartridge Refills because they were distributed with incorrect packaging and Instructions for Use.
Olympus is recalling 335 PowerSeal 5 mm Sealer & Divider devices because the outer shelf box is incorrectly labeled as a 37-cm device.