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.
Grato Holdings, Inc. is recalling 850 bottles of HGH Vitality Homeopathic tablets due to an error on the declared strength.
Sundial Herbal Products is recalling Sarsaparilla herbal products under a permanent injunction because the items are misbranded and deemed unapproved drugs.
Sundial Herbal Products is recalling Sundial Traditional African Manback Tonic because the product is misbranded and deemed an unapproved drug based on its labeling claims.
Sundial Herbal Products is recalling Guava Leaf herbal products because they are misbranded and deemed unapproved drugs based on labeling claims.
Sundial Herbal Products is recalling Fig Leaf herbal products under a permanent injunction because the labeling makes unapproved drug claims.
Sundial Herbal Products is recalling Sundial Organic Jamaican Turmeric because the product is misbranded and deemed an unapproved drug due to labeling claims.
Sundial Herbal Products is recalling Fever Grass herbal products under a court order because the labels make unapproved drug claims.
Keurig Dr Pepper is recalling Newman's Own Organic Decaf Ground Coffee because it contains regular non-organic coffee. Consumers should stop using the product.
Sundial Herbal Products is recalling Sundial Ethiopian Tenadam Herb because the product is misbranded and deemed an unapproved drug based on its labeling claims.
Stimwave Technologies is recalling 2,197 StimQ Peripheral Nerve Stimulator units because they contain a non-functional component not listed in the product labeling.
Sundial Herbal Products is recalling Sea Moss/Irish Moss products because they are misbranded and deemed unapproved drugs based on labeling claims.
Sundial Herbal Products is recalling Koromantee Colonic & Intestinal Cleaner because the product is misbranded and deemed an unapproved drug based on its labeling claims.
Sundial Herbal Products is recalling Jamaican Milk Wiss herbal products because they are misbranded and deemed unapproved drugs based on labeling claims.
Sundial Herbal Products is recalling Sundial Hemp Seed Oil because the product is misbranded and deemed an unapproved drug based on its labeling claims.
Stimwave Technologies is recalling 1,424 StimQ Peripheral Nerve Stimulator units because they contain a non-functional component not referenced in product labeling.
Sundial Herbal Products is recalling its Traditional Herbal Formula for Asthma because it is an unapproved drug with misbranded labeling.
Sundial Herbal Products is recalling Mango Leaf herbal products because they are misbranded and deemed unapproved drugs based on labeling claims.
Leiper's Fork Distillery is recalling 1,996 gallons of 70% Ethyl Alcohol Antiseptic Topical Solution because the product is labeled to contain methanol.
Sundial Herbal Products is recalling Red Water Grass herbal products under a permanent injunction because the items are misbranded and deemed unapproved drugs.
Sundial Herbal Products is recalling its Traditional Herbal Formula for Diabetics because the product is misbranded and considered an unapproved drug.
Sundial Herbal Products is recalling Wood and Root Tonic under a permanent injunction because the product is misbranded and deemed an unapproved drug.
Sundial Herbal Products is recalling Broom Weed herbal products under a permanent injunction because the items are misbranded and deemed unapproved drugs.
SCA Pharmaceuticals is recalling Heparin Sodium 5,000 units in 0.9% Sodium Chloride 1000 mL single-dose containers due to cross-contamination with undeclared benzyl alcohol.
SCA Pharmaceuticals is recalling Heparin Sodium 10,000 units injection containers due to cross contamination with undeclared benzyl alcohol and missing parabens.
Fantis Foods is recalling frozen pita bread because the packaging fails to declare milk as an allergen, despite listing whey in the ingredients.