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.
Campos Foods is recalling approximately 126,705 pounds of H-E-B beef cheese burgers because they contain undeclared wheat, a known allergen.
Sunset Farm Foods is recalling approximately 42,669 pounds of link sausage products due to misbranding and an undeclared soy allergen.
My Sweet Ol' Etcetera is recalling 36 units of Mint Bars due to undeclared wheat and soy lecithin. The product was distributed in Oregon.
My Sweet Ol' Etcetera is recalling 36 units of Peanut Butter Brownies distributed in Oregon due to undeclared soy lecithin.
Biomet is recalling specific acetabular shell components for hip prostheses due to a packaging mix-up between two different product lots.
Biomet is recalling 17 units of the Mallory Head 4 Finned Acetabular Shell 50 mm (Lot 364600) due to a packaging mix-up with a different shell size.
Teleflex is recalling RUSCH Curved Reinforced Endotracheal Tubes because the labeled cuff diameter does not match the actual cuff diameter, though the actual product meets specifications.
Intuitive Surgical is recalling 12,467 Harmonic Ace Curved Shears Instructions for Use because they incorrectly instruct users on how to manually open the grips.
Intuitive Surgical is recalling Harmonic Ace Curved Shears Instructions for Use because they incorrectly instruct users on how to manually open the grips.
Son In Law Products is recalling Medium Smoking BBQ Sauce and other varieties because they contain anchovies not listed on the label.
Damon Industries is recalling Fruitful Juice Bloody Mary Beverage Concentrate because it contains anchovies that were not declared on the label.
Damon Industries is recalling Bloody Mary Beverage Concentrate because it contains anchovies that were not declared on the label.
Son In Law Products is recalling three varieties of BBQ sauce because they contain anchovies that are not listed on the label.
Son In Law Products is recalling Hot & Medium Smoking BBQ, Garlic & Honey horseradish BBQ, and Cherry BBQ Sauces because they contain anchovies not declared on the labeling.
Mt. Rose Drinks is recalling Bloody Mary mixes because Worcestershire sauce contains anchovies not listed on the label.
SCC Soft Computer is recalling specific versions of the SoftPath Laboratory Information System because diagnostic text modifications may not be saved or displayed correctly.
Damon Industries is recalling Bloody Mary beverage concentrate because Worcestershire sauce used in the product contains anchovies that were not declared on the label.
Damon Industries is recalling 87 gallons of Southern Supreme Spicy Tabasco Bloody Mary Beverage Concentrate because it contains undeclared anchovies.
Son In Law Products is recalling Cherry BBQ Sauce because it contains anchovies that are not listed on the label.
Teleflex Medical is recalling 300 units of preformed tracheal tubes because they are incorrectly labeled as cuffed oral tubes instead of uncuffed nasal tubes.
Stryker is recalling MEDPOR Titan Max Orbital Floor and Wall implants due to incorrect barrier location and potential mix-ups with left-sided units.
HVL, LLC is recalling 278 bottles of Melatonin Control-Released Tablets that contained a vegetarian digestive enzyme instead of melatonin.
Teleflex Medical is recalling 2,640 units of LMA Supreme (New Cuff) Size 5 devices because some may be mislabeled as Size 5 but are actually Size 4.
MAST Biosurgery is recalling 49 units of SurgiWrap Bioresorbable Adhesion Barrier Film because the expiration date on the barcode did not match the printed date.
Stryker is recalling Flyte Togas with an incorrect expiration date. The label reads 2412-12-01 instead of 2014-12-01.