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.
Breg Inc is recalling two knee support models because they contain latex but lack the required caution label.
Breg Inc is recalling specific knee sleeves because they contain latex but lack the required caution labels.
Fannie May Confections Brands, Inc. is recalling specific lots of Assorted Chocolates because the ingredient statement fails to declare peanuts.
Keen-Wah LLC is recalling i heart keenwah Ginger Peanut All Natural Quinoa Clusters because an anti-stick spray containing soy lecithin was used during manufacturing, but soy was not declared on the label.
Northern Valley Baking Co. is recalling G'nache P'nache products because milk and soy were not declared on the allergen statement.
Keen-Wah LLC is recalling i heart keenwah Chocolate Sea Salt All Natural Quinoa Clusters because soy was not declared on the label.
Intuitive Surgical is recalling 5,217 5mm Curved Cannulae for the da Vinci Si Surgical System due to potential damage during use and to update labeling instructions.
Agila Specialties Private Ltd. is recalling etomidate injection vials due to potential particulate matter and missing or illegible lot and expiry date labels.
Remington Medical is recalling FAS-LOC 6 Foot Disposable Extension Cables because the instruction manual incorrectly displays the polarity for the black connector.
Novartis is recalling Ritalin tablets because the attached Medication Guide contained information for the sustained-release version. The recall is limited to a specific lot distributed nationwide and in Puerto Rico.
Hospira Inc. is recalling 237,850 ampoules of Demerol (meperidine HCL) because the immediate container labels are missing. The recall is nationwide.
Novartis is recalling 10,781 bottles of Ritalin 20 mg tablets because the attached Medication Guide contained information for Ritalin SR instead of Ritalin Tablets.
Forest River is recalling 164 model year 2014 Vibe travel trailers because the Federal Certification Label lists incorrect tire and weight information, which could lead to overloading and tire failure.
Merit Medical Systems is recalling 15 syringe kits labeled as sterile but not sterilized. The products were distributed in the US, Thailand, and Hong Kong.
Ormco/Sybronendo is recalling 150 Spirit MB Orthodontic Brackets because a misplaced ID dot may cause incorrect tooth placement.
Butter Creek Farms is recalling Oatmeal Raisin Cookies due to undeclared wheat and egg. The cookies were sold online and at two retail stores in Washington.
Whole Foods Market is recalling Tom Yom Soup because the ingredient list includes whey but fails to declare milk as the source of the allergen.
Unilever is voluntarily recalling specific Popsicle ice pop boxes because they may have been exposed to milk, an ingredient not listed on the label.
Butter Creek Farms is recalling Snickerdoodle Cookies due to undeclared wheat and egg. The cookies were sold online and at two retail stores in Washington.
Stryker Howmedica Osteonics is recalling 48 Citation V40 Hip Stems because a left-sided implant was found in packaging labeled for a right-sided implant.
Technidata S.A. is recalling TDWorkstation software versions 11.01.A and higher because a conflict may cause the system to send incorrect patient demography to connected instruments.
Ormco is recalling 150 units of Titanium Orthos Brackets because the color identification dot was marked on the wrong tie-wing.
Abbott Point of Care is recalling i-STAT G3+ Cartridges (Lot N13183) because they may produce incorrectly elevated PCO2 and depressed pH results.
Creole Delicacies Kitchens Inc is recalling Cookin' Cajun Acadiana Style Etouffee Seasoning Blend because it contains undeclared wheat flour.
Bard Access Systems is recalling 777 PowerPort Slim Implantable Ports because the labels incorrectly state they contain silicone suture plugs, when some units do not.