Hazard
9,606 recalls in our database tag this hazard, drawn from FDA, USDA FSIS, CPSC, and NHTSA source notices.
Of the 9,606 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.
Medline Industries is recalling 8,250 units of sterile PVP solution distributed nationwide because the contents are non-sterile despite being labeled as sterile.
Medline PVP Solution (REF DYNDA1858) is being recalled because it is labeled as sterile but contains non-sterile contents. 1,950 units are affected.
Medline Industries recalls 300 units of Sterile Povidone (REF DYNDA2061) after discovering the solution inside foil sachets is non-sterile despite sterile labeling. Affected lots are distributed across eight states.
Medline STERILE PVP SLN KIT (Lot 21GBJ087) is recalled because its contents are non-sterile despite labeling stating sterile product. Consumers should stop use immediately.
Gaws Gourmet Foods is recalling Gaw's Classic Italian sub due to undeclared sesame. The recall affects 699 units distributed in Michigan; consumers who are allergic to sesame should not consume the product.
The CARDIOHELP-i Heart-Lung Support System is recalled because factory settings were incorrectly described in the manual. Healthcare providers should verify device settings with the manufacturer.
Medtronic is recalling 2,543 SynchroMed Model A10 infusion pumps with software version 1.1.300 due to missing decimal separators on parameter display screens. The omission could lead to misinterpretation of dosing parameters.
Limacorporate is recalling 33 PHYSICA HPS Tibial Liner units distributed in the U.S. due to incorrect product labeling. No adverse events have been reported.
E.A. Sween Co. is recalling Deli Express Deli Club sandwiches (lot U023236) due to label mix-up with inaccurate required label information. The recall affects 31,550 units distributed across 19 states.
Great Dane is recalling 2023 Champion trailers because incorrect VINs on certification labels may prevent owners from recognizing safety recalls.
Traeger is recalling about 37,000 Flatrock Flat Top Propane Grills because burner control knobs can be incorrectly labeled, allowing the grill to be unintentionally left on and posing a fire hazard. No fires or injuries have been reported.
BAPS Shayona is recalling Kesar Penda Ricotta fudge discs because they contain undeclared soy and Yellow #5 & #6 dyes. The product was distributed to six Southern states.
Hans Kissle Potato Salad White Homestyle (10 lb. bulk cases) is being recalled for undeclared egg and soy allergens. The recall affects units distributed in Connecticut and Massachusetts with a use-by date of November 25, 2023.
BAPS Shayona is recalling 723 units of Plain Penda Ricotta fudge discs because some contain undeclared soy. The product was distributed to six states and poses a risk for those with soy allergies.
BAPS Shayona Kaju Pista Roll sweet rolls are being recalled because they contain undeclared Yellow #5, Yellow #6, and Blue 1 food dyes. The recall affects 138 units distributed to six southern states.
The CPSC has recalled about 2,000 Vibe Bear playyard mattresses sold on Amazon.com from January to June 2023 due to suffocation hazard to infants. The mattresses violate federal crib mattress safety regulations and lack required warnings and labels.
USDA FSIS issued a public health alert for Whole Foods Market Kitchens soup mislabeled as beef, containing undeclared sesame.
Bonta Natural Artisan Gelato Stracciatella is being recalled due to undeclared soy lecithin. Soy is a major allergen; consumers with soy allergies should not consume this product.
Glenmark Pharmaceuticals is recalling 37,200 bottles of Indomethacin 25mg capsules distributed nationwide because the bottles may be labeled as Naproxen instead. This labeling error could cause medication confusion.
Bisousweet Confections is recalling certain Chocolate Whoopie Pie packages that contain Raspberry Whoopie Pies instead. Consumers should not consume the recalled products.
Certain 2024 Volvo VN and VHD trucks have an incorrect Gross Axle Weight Rating label, which can allow vehicles to be overloaded and increases crash risk. Dealers will replace the label free of charge.
Certain BD Extension Sets sold as free of DEHP (di(2-ethylhexyl) phthalate) actually contain this restricted phthalate. The products have been distributed worldwide.
Certain lots of AVANOS BALLARD Closed Suction System for Adults were labeled as DEHP-free but contain DEHP in tubing components. These units are used for mechanical ventilation and distributed in the US and South Africa.
BD gravity blood infusion sets labeled as free of DEHP (di(2-ethylhexyl) phthalate) actually contain the substance. The recall affects products distributed worldwide through July 31, 2026.
BD Alaris Pump infusion sets labeled as DEHP-free actually contain di(2-ethylhexyl) phthalate. The worldwide recall affects multiple catalog numbers distributed throughout the US and internationally.