Hazard
9,622 recalls in our database tag this hazard, drawn from FDA, USDA FSIS, CPSC, and NHTSA source notices.
Of the 9,622 mis labeling recalls we have scored against our rubric, 163 (2%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 590 (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.
Paleteria Y Neveria La Rosita, LLC is recalling 4 oz. Strawberry Fruit Bars sold in Michigan and Indiana because the product contains undeclared FD&C Blue # 1.
Physicians Total Care is recalling one bottle of Percocet 10/325 mg tablets because it contained a foreign Endocet 10/25 mg tablet.
Paleteria Y Neveria La Rosita, LLC is recalling 4 oz. Strawberry Eskimo Dessert Bars because the product contains undeclared FD&C Blue # 1.
Paleteria Y Neveria La Rosita, LLC is recalling Pina Colada Dessert Bars because the product contains undeclared FD&C Red #40.
Triumph is recalling 2012-2013 Explorer and Explorer XC motorcycles because incorrect Gross Vehicle Weight Rating labels may lead to overloading and increased crash risk.
Beckman Coulter is recalling 490 AU5800 Clinical Chemistry Analyzers due to a software error that may cause the system to misidentify samples and report erroneous patient results.
All One, Inc. is recalling multiple vitamin powder canisters because the label incorrectly claims 'No Dairy' and 'Certified Vegan' despite containing milk.
All One, Inc. is recalling 796 units of Active Senior Multiple Vitamin & Mineral Powder because the label incorrectly claims 'No Dairy' and 'Certified Vegan' despite containing whey protein isolate.
Meijer Distribution is recalling 1,080 units of Essential M with Real Strawberries because the label fails to identify soy lecithin, a potential allergen.
SIB, Inc. is recalling specific lots of Bakehouse Granola because the packaging fails to list milk as an ingredient, posing a risk to consumers with milk allergies.
DePuy Mitek is recalling Blue Orthocord sutures because the instructions for use incorrectly state they retain 100% strength at six weeks, when they actually retain approximately 80%.
DePuy Mitek is recalling ORTHOCORD sutures because the instructions for use incorrectly state that Blue sutures retain 100% strength at six weeks.
DePuy Mitek is recalling Blue Orthocord sutures because the instructions for use incorrectly state that 100% suture strength remains at six weeks.
DePuy Mitek is recalling ORTHOCORD sutures because the instructions for use incorrectly state that Blue sutures retain 100% strength at six weeks.
OPMX, LLC is recalling Pentrexcilina Jarabe NF liquid because its label may be confused with Pentrexyl, a prescription antibiotic.
DePuy Mitek is recalling ORTHOCORD sutures because the instructions for use incorrectly state that Blue sutures retain 100% strength at six weeks.
Ozone Confection & Bakers Supply Co. is recalling 481 units of Non-Pareil Seeds because they contain undeclared FD&C colors.
Stellate Systems is recalling Harmonie software versions 5.1 to 6.2e because the product's labeling indications have not been cleared by the FDA for sale in the USA.
OPMX, LLC is recalling Pentrexcilina tablets because the labels are misleading and may be confused with a prescription antibiotic.
Ozone Confection & Bakers Supply Co. is recalling 481 boxes of Non-Pareil Seeds because they contain undeclared FD&C colors.
Ozone Confection & Bakers Supply Co. is recalling 481 units of Easter Mix Non-Pareil Seeds because they contain undeclared FD&C colors.
Sirtex Medical Limited is recalling 21 doses of SIR-yttrium 90 microspheres due to an incorrect expiration date. The product is used to treat unresectable metastatic liver tumors.
Mylan Pharmaceuticals is recalling 2,405 bottles of Lisinopril 10 mg tablets because the pills have the wrong ID code imprinted on them.
Precision Dose Inc. is recalling Children's Acetaminophen Oral Suspension because the label is misleading. The product contains an adult dose of acetaminophen despite the name.
Intuitive Surgical is recalling IS2000 user manuals for the da Vinci S system to provide revised instructions on sterile adapter engagement and instrument installation.