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.
Mondelez Global LLC is recalling 1.9 lb bags of Sour Patch Kids because peanut shell remnants were found in two containers. The product is not labeled as containing peanuts.
Teleflex Medical is recalling Visistat 35 skin closure devices because some boxes are mislabeled as Wide when they contain Regular devices.
Medical Components, Inc. is recalling 8F Plastic Dignity Low Profile CT Port kits because they were packaged with unmarked guidewires instead of the marked ones indicated on the label.
Mesa Laboratories is recalling specific lots of ProSpore Biological Indicators because the concentration of bromocresol purple does not conform to specification.
Johnson & Johnson is voluntarily recalling select first aid wraps because the 'not made with natural rubber latex' label is inaccurate.
Johnson & Johnson is recalling select COACH Self-Adhering Sports Wraps because the label incorrectly states they are not made with natural rubber latex.
Johnson & Johnson is recalling select first aid wraps because they were labeled as latex-free but used natural latex in early manufacturing.
Johnson & Johnson is voluntarily recalling select first aid wraps because the label incorrectly states they are not made with natural rubber latex.
Johnson & Johnson is recalling COACH Self-Adhering Sports Wraps because the label incorrectly states they are not made with natural rubber latex, though latex was used in early manufacturing.
Zimmer Dental Inc is recalling Tapered Screw-Vent MTX dental implants because two lots were inadvertently commingled during manufacturing, potentially resulting in mislabeling.
Zimmer Biomet is recalling 12 hip implant packages labeled as size 7.5 that actually contained size 4 implants.
Johnson & Johnson is voluntarily recalling select first aid wraps because the packaging incorrectly states they are not made with natural rubber latex.
Getinge US Sales LLC is recalling Hemashield Knitted Double Velour Cardiovascular Fabric because the packaging label lists a different product size than the actual item inside.
Mesa Laboratories is recalling SporAmpule Biological Indicators because the concentration of bromocresol purple does not conform to specification.
Zimmer Dental Inc is recalling Tapered Screw-Vent MTX dental implants because two lots with different thread diameters were commingled and may be mislabeled.
Nestle Dreyers is recalling 30 cases of Dreyer's Slow Churned Vanilla Bean Ice Cream in Colorado because the cartons contain Butter Pecan ice cream.
PepsiCo is recalling 1,296 cases of Diet Pepsi 12-packs in Arizona due to mislabeling. No illnesses have been reported.
PepsiCo is recalling 194 cases of Diet Pepsi Caffeine Free because the outer packaging incorrectly states 'Aspartame Free' while the product contains aspartame.
Glenmark Pharmaceuticals is recalling Indomethacin Capsules 50 mg because the bottles display incorrect adult dosage instructions.
Keystone Dental Inc is recalling 55 units of plastic abutment sleeves that were packed as non-locking but are actually locking.
NxStage Medical is recalling 1,243,400 units of PureFlow B Solution because the original labeling failed to warn against mixing dialysate formulations.
Merit Medical Systems is recalling 30 Flex-Neck Classic Peritoneal Dialysis Catheters because 2-cuff devices were incorrectly configured and labeled as 1-cuff products.
Centurion Medical Products Corporation is recalling Wound Closure Tray - Facial devices due to a Class II FDA recall.
Smiths Medical ASD Inc. is recalling Medfusion Syringe Pumps because they may fail to recognize or misidentify loaded medication syringes, potentially preventing proper pump programming.
Smiths Medical is recalling Medfusion Syringe Pumps because they may fail to recognize or misidentify loaded medication syringes, preventing proper programming.