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.
NutraBlend Foods is recalling Russian Bear 10000 Weight Gainer Formula because it contains undeclared soy protein isolate.
Philips is recalling 2,214 MRI Patient Monitoring Systems because the instructions for oxygen sensor calibration are incorrect for specific software versions.
Qiagen Sciences LLC is recalling AmniSure ROM Test kits because the packaging displays an incorrect rinse time of 30 seconds instead of the correct 1 minute.
Conformis, Inc. is recalling four iTotal CR Knee Replacement System kits because they were labeled with incorrect serial numbers and delivered to the wrong customers.
Conformis is recalling two iTotal PS Knee Replacement System kits because tibial trays were labeled with incorrect serial numbers and delivered to the wrong customers.
Haemonetics is recalling TEG Manager software versions 1.1.0 through 4.1.1 because a defect causes incorrect out-of-range alerts for coagulation test results.
National Vitamin Company is recalling Nature's Blend Folic Acid 1000 mcg bottles due to a front panel label error stating 1000 mg instead of 1000 mcg.
Keystone RV Company is recalling 2018-2020 Crossroads Hampton 371FKL trailers because the Federal Identification Tag incorrectly lists tire pressure as 6 PSI instead of 80 PSI.
Southern Sisters Gourmet Taco Soup is being recalled because it contains undeclared milk and soy. The product was distributed in nine states.
Southern Sisters Gourmet is recalling Caramel Apple Cobbler because it contains wheat, an allergen not listed on the label.
Biomet is recalling 14 units of 9mm Shoulder Mini Humeral Stems that were misidentified as 15mm units. The error poses a risk of improper surgical implantation.
Karl Storz is recalling 42 flexible neuroscopes because the instruction manual contains incorrect sterilization information for the STERIS System 1E, which may compromise sterility.
Randox Laboratories is recalling Chemistry QC Premium Plus due to incorrect Sodium target values. The error affects quality control accuracy for diagnostic assays.
Glaxosmithkline is recalling specific lots of Advil Allergy and Congestion Relief tablets because they lack required safety warning information in the Drug Facts Panel.
Medtronic is recalling two Open Pivot Aortic Valve Grafts because the outer box was mislabeled as Aortic while the device was Mitral.
GlaxoSmithKline is recalling specific lots of Advil Allergy and Congestion Relief because the Drug Facts Panel lacks required safety warning information.
Elekta Impac Software is recalling MOSAIQ oncology software because users may enter metric values into fields labeled with US standard units.
American Classic Snack Company is recalling Sweet Bourbon Crunchers Pretzels because they are improperly labeled with a gluten-free claim.
Corinthian Trading Inc. is recalling uncooked sweet potato crusted Alaska pollock nuggets because the product contains chicken nuggets instead of fish.
Nostrum Laboratories is recalling Theophylline Extended-Release Tablets because poor manufacturing practices resulted in incorrect lot and expiration date labeling.
Cook Inc. is recalling 25 Spectrum Central Venous Catheter Trays because the printed expiration dates are incorrect. The devices were distributed to seven US states and Canada.
Beckman Coulter is recalling iChemVELOCITY Strips because the Leukocyte and Compensation pads were switched on some vials of lot 7212269M.
Glaxosmithkline is recalling 446,628 bottles of Advil Liqui-Gel Minis because certain lots lack required safety warning information in the Drug Facts Panel.
Glaxosmithkline is recalling specific lots of Infants Advil (Ibuprofen) because the Drug Facts Panel lacks required safety warning information.
Glaxosmithkline is recalling specific lots of Advil Liqui-Gel Mini because the Drug Facts Panel lacks required safety warning information.