Hazard
9,611 recalls in our database tag this hazard, drawn from FDA, USDA FSIS, CPSC, and NHTSA source notices.
Of the 9,611 mis labeling recalls we have scored against our rubric, 161 (2%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 589 (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.
Chemi-Source Inc. is recalling Delicious Whole-istic Whey Protein Duch Chocolate because the milk allergen was not listed on the label.
LL Bakery is recalling specific breads and pastries because the labels fail to declare milk as an allergen.
Chemi-Source Inc. is recalling Metabolic Whey protein products because milk and soy allergens were not properly labeled. Consumers with allergies to these ingredients should stop using the product.
Chemi-Source Inc is recalling All Natural Whey protein products because the milk allergen was not listed on the label.
Sprouts Farmers Market Whey Protein Vanilla is being recalled because the whey ingredient is not listed as milk, a major allergen. Consumers with milk allergies are at risk of serious allergic reactions.
LL Bakery is recalling specific bread and Danish products because the labels fail to declare milk as an allergen in the whey powder.
Chemi-Source Inc. is recalling Metabolic Whey protein powder because the packaging fails to list milk and soy as ingredients. Consumers with allergies to these substances are at risk of serious allergic reactions.
Chemi-Source Inc is recalling Isolate Whey Protein Chocolate Malt because the whey ingredient was not listed as milk, a major allergen.
Chemi-Source Inc is recalling Fruit-N-Whey protein powder because the whey ingredient was not listed as a milk allergen, posing a risk to consumers with milk allergies.
Chemi-Source Inc. is recalling Flax-N-Whey products because the whey ingredient contains milk, a major allergen, that is not listed on the label.
Chemi-Source Inc. is recalling 1,320 units of 100% Micellar Casein powder because the milk ingredient was not listed as an allergen.
Coloplast is recalling three lots of Digitex Absorbable Polydiaxanone Sutures because they are mislabeled with a three-year expiration date.
Biomet is recalling 8 units of Active Articulation E1 hip bearing implants because outer and inner labels display incorrect or conflicting outer diameter sizes.
Invatec Llc is recalling 177 Diver C.E. aspiration catheters because the labeled indications for use were not included in the existing regulatory clearance.
Optovue, Inc. is recalling iVue software versions 3.0 and 3.1 because color displays for Ganglion Cell Complex thickness are inconsistent across different report types.
Bion Enterprises is recalling 504 units of IgG FITC Conjugate because the labeled expiration date is one year too long.
Bion Enterprises is recalling 201 units of IgM Conjugate because the labeled expiration date is one year too long.
Physicians Total Care is recalling 76 tubes of Voltaren 1% Gel because the lot number and expiration date on the tubes may not be legible.
Novartis is recalling Target Up & Up athlete's foot cream because the lot and expiration dates on the tubes may not be legible.
Novartis Consumer Health is recalling Voltaren Gel because lot and expiration dates on the tubes may be illegible. The FDA classifies this as a Class III recall.
Bion Enterprises Ltd is recalling 207 units of IgG Conjugate because the labeled expiration date is one year too long.
Novartis is recalling 219,600 tubes of Lamisil AT Cream because the lot and expiration dates may be illegible.
Legacy Pharmaceutical Packaging LLC is recalling 1,644 bottles of Lorazepam 0.5 mg tablets because of incorrect or missing lot and expiration dates.
Novartis Consumer Health is recalling specific lots of Lamisil AT Cream because the lot and expiration dates on the tubes may be illegible.
Novartis is recalling Lamisil AT Cream because the lot and expiration dates on the tubes may be illegible. The recall covers 12-gm and 30-gm tubes distributed nationwide, in Puerto Rico, and in Panama.