Hazard
9,607 recalls in our database tag this hazard, drawn from FDA, USDA FSIS, CPSC, and NHTSA source notices.
Of the 9,607 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.
Arrow International is recalling 1,351 CG+ Arrow PIC Catheters due to a labeling error where lidstock and banner card codes do not match.
Philips Healthcare Inc. is recalling 220 Mobile Diagnostic X-Ray Systems because electronic markers may be placed at the wrong anatomical position when images are moved between views.
Beckman Coulter is recalling Rack ID Labels for AU680 and AU5800 analyzers because the displayed ID number and barcode do not match.
Intuitive Surgical is recalling da Vinci Xi Stapler Release Kits because misinterpretation of instructions may result in tool damage.
Intuitive Surgical is recalling da Vinci Xi Stapler Release Kits because misinterpreted instructions may cause tool damage.
Intuitive Surgical is recalling da Vinci Xi EndoWrist Stapler Release Kits because misinterpretation of instructions may result in tool damage.
Intuitive Surgical is recalling da Vinci Xi EndoWrist Stapler Release Kits because misinterpretation of instructions may result in tool damage.
Intuitive Surgical is recalling da Vinci Xi EndoWrist Stapler Release Kits because misinterpreted instructions may cause tool damage.
Intuitive Surgical is recalling da Vinci Xi EndoWrist Stapler Release Kits because misinterpretation of instructions may result in tool damage.
Intuitive Surgical is recalling da Vinci Xi EndoWrist Stapler Release Kits because misinterpretation of instructions may result in tool damage.
Intuitive Surgical is recalling da Vinci Xi Stapler Release Kits because misinterpreted instructions may cause tool damage.
Intuitive Surgical is recalling da Vinci Xi EndoWrist Stapler Release Kits because misinterpretation of instructions may result in tool damage.
G & W Laboratories is recalling 230,700 tubes of Ciclopirox Olamine Cream because some lots were packaged with an out-of-date package insert.
Thor Motor Coach is recalling 2017 Ace, Hurricane, and Windsport motorhomes because tow hitch labels incorrectly state a 10,000 lb capacity instead of the actual 8,000 lbs.
Thor Motor Coach is recalling 2017 Palazzo 36.1 and 36.3 motorhomes because the federal certification label lists an incorrect front tire rim size, which could lead to unsafe driving conditions if the rim is replaced based on that error.
Forest River is recalling 2007-2011 Cherokee recreational trailers because incorrect Federal Placards list higher weight ratings than the actual capacity, increasing the risk of overloading and crashes.
Forest River is recalling 2017 Rockwood and Flagstaff recreational vehicles because the Federal Placard may display an incorrect Gross Axle Weight Rating, which could increase crash risk.
Kusher LLC is recalling Cookies Nezhakomka because the label fails to declare milk, a major allergen, despite the product containing butter.
Kusher LLC is recalling Princesa cookies because the label fails to declare milk, a major allergen, despite the product containing butter.
Data Innovations, LLC is recalling JResultNet software because a defect may cause one patient's test results to be associated with another patient.
Kusher LLC is recalling Cookies Prince packages because the label fails to declare milk, a major allergen present in the product as butter.
Meijer is recalling pre-made Caesar salads that were mislabeled as Greek salads and contain undeclared wheat. The affected products were distributed in six states.
Kusher LLC is recalling Cookies Assorti because the packaging failed to list egg and milk in the 'Contains' statement, posing a risk to allergic consumers.
Bitterman and Sons is recalling Parmesan Truffle Salt because the label declares Parmigiano Reggiano cheese but fails to list milk as an ingredient.
Kusher LLC is recalling 476 packages of Cookies Fantazia because the label failed to declare egg and milk allergens. The product was distributed in California, Oregon, and Washington.