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.
Conagra Inc is recalling Andy Capp's Cheddar Cheese Fries because they were packaged in Hot Fries bags that do not list soy as an ingredient.
Ansell Healthcare Products LLC is recalling one lot of Lifestyles Pleasure Collection condoms because Ultra Thin condoms were included instead of the labeled Skyn style.
Cardinal Health is recalling specific lots of Dairy Aid Lactase Enzyme Supplement caplets because the packaging incorrectly lists the strength as 9,000 FCC Units instead of 3,000 FCC Units.
Medisystems is recalling 17 Gauge AV Fistula Needles because single needle packs are mislabeled as 15 Gauge. The recall covers 4,000 needles distributed in New York, Pennsylvania, and Tennessee.
Pepsi Cola North America is recalling Regular and Diet Wild Cherry Pepsi two-liter bottles because labels were swapped during production, posing a risk to individuals with phenylketonuria or diabetes.
Abbott Point of Care Canada Limited is recalling 10 boxes of i-Stat cTnI cartridges from lot P12179 due to incorrect barcodes on the cartridge portion pack.
Medisystems is recalling 5 mislabeled buttonhole needle pouches that were labeled as 15 Ga x 1 inch instead of 15 Ga x 3/5 inch.
Woodstock Farms is recalling Tamari Almonds because the label fails to list soy, a major allergen, posing a risk of severe allergic reactions.
Somersault Snack Co. is recalling Cinnamon Crunch sunflower seed snacks because the packaging failed to declare a milk allergen present in a flavor ingredient.
Unilever is recalling Knorr Pasta Sides Cheesy Bacon Macaroni because some pouches may contain soy due to a packaging error.
Sugar Flowers Plus is recalling Pastillage Flowers because they contain undeclared egg white wash used as a glue.
Sugar Flowers Plus is recalling Pastillage Flowers because they contain undeclared egg white wash used as glue.
Sugar Flowers Plus is recalling Pastillage Flowers because they contain undeclared egg white wash used as glue.
Sugar Flowers Plus is recalling Pastillage Flowers because they contain undeclared egg white wash used as a glue.
Sugar Flowers Plus is recalling Pastillage Flowers because they contain undeclared egg white wash used as glue.
Sugar Flowers Plus is recalling Pastillage Flowers because they contain undeclared egg white wash used as glue.
Sugar Flowers Plus is recalling Pastillage Flowers because they contain undeclared egg white wash used as glue.
Quanta System is recalling 75 Q-Plus T laser units because promotional materials on their website did not specify that certain claims did not apply to U.S. distributed devices.
James G. Cole, Inc. is recalling I-C Drops Eye Cleansing Agent because the label does not state the product is sterile, as required by FDA regulations.
Quanta System is recalling 12 Eterna Giovinezza laser units because its website contained promotional materials with claims not applicable to U.S. distributed devices.
Quanta System is recalling 22 laser surgical instruments because website promotional materials contained claims not applicable to US devices.
IDS is recalling 25-Hydroxy Vitamin D EIA kits because a quality control report contained an incorrect calibrator value.
Philips is recalling 108 CT systems because a software defect prevents users from labeling coronary arteries in rendered images.
Upsher Smith is recalling 11,316 bottles of Divalproex Sodium Delayed-Release Tablets because some labels are missing the color-coded strength indicator.
UNFI is recalling Kinnikinnick Gluten-Free Pie Crusts because they contain eggs that are not listed on the label.