Hazard
9,622 recalls in our database tag this hazard, drawn from FDA, USDA FSIS, CPSC, and NHTSA source notices.
Of the 9,622 mis labeling recalls we have scored against our rubric, 163 (2%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 590 (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.
Entegra Coach is recalling 2013 Aspire motorhomes because the certification label incorrectly identifies rear axle tire sizes, potentially leading to improper tire installation.
Siemens Healthcare Diagnostics is recalling specific lots of TSH calibrator vials because they showed under-recovery of dose values.
New B.C.N. Trading Inc. is recalling Asian Boy Tapioca Sticks because they contain undeclared sulfites. The product was distributed in six states.
Dawn Food Products is recalling Sam's Club Artisan Fresh Miniature Candy Cookies due to a labeling discrepancy involving White Chocolate Macadamia Nut Cookies.
Stryker is recalling specific Accolade hip stems because size 3.5 stems were mistakenly packaged as size 2.5 stems, creating a risk of product mix-up.
Philips is recalling HeartStart FRx AEDs to clarify maintenance instructions in the Owner's Manual.
Siemens is recalling CLINITEK Atlas Positive and Negative Control Strips because leukocyte results may become negative if the solution is held above 25°C for more than two hours.
Siemens Healthcare Diagnostics is recalling specific lots of Emit 2000 and Syva Emit Phenobarbital Assays due to higher imprecision and outliers on Beckman Coulter AU Systems.
Siemens Healthcare Diagnostics is recalling 1,998 cartons of Emit Tox Serum Calibrators because an incorrect expiration date was assigned to Lot D1.
Siemens Healthcare Diagnostics is recalling specific lots of Coat-A-Consta IRMA TSH calibrators due to confirmed under-recovery of dose values.
Siemens Healthcare Diagnostics is recalling specific lots of Chek-Stix control strips because the leukocyte result may become negative if the solution is held above 25°C for more than two hours.
Siemens Healthcare Diagnostics is recalling Chek-Stix control strips because the leukocyte result may become negative if the solution is held above 25°C for more than two hours.
Meijer Distribution is recalling 16oz Redskin Peanuts because sodium content was not correctly stated on the label. No illnesses have been reported.
Siemens Healthcare Diagnostics is recalling specific lots of TSH calibrator vials because they showed under-recovery of dose values and a darker yellow color.
Siemens Healthcare Diagnostics is recalling Chek-Stix Combo Pak control strips because the leukocyte result may become negative if the solution is held above 25°C for more than two hours.
Mindray is recalling two DPM Central Station units due to a software anomaly that may replace one patient's trend data with another's.
Nature's Path Foods is recalling 25 lb. containers of Hemp Plus Granola because the product contains almonds that are not declared on the label.
Natural Organics is recalling Nature's Plus Spiru-tein High Protein Energy Meal, S'mores flavor, because it is labeled gluten-free but contains gluten.
Fleetwood RV is recalling 2012-2013 Bounder Classic motorhomes because incorrect federal certification tags may lead to improper tire inflation and potential tire failure.
Abbott Laboratories is recalling specific lots of Synthroid (levothyroxine sodium) tablets because bottles labeled as 150 mcg actually contained 75 mcg tablets.
HemoCue AB is recalling 48 urine analyzers because they were shipped with the wrong Quick Reference Guide and a missing warranty statement.
St. Jude Medical is recalling 26 units of Fast-Cath Transseptal Guiding Introducers because they were packaged with a 180-degree curve instead of the labeled 90-degree curve.
Golub Corp is recalling CMC Cinnamon Coffee Cakes incorrectly labeled as Pumpkin Coffee Cake, which failed to list walnuts as an ingredient.
Beckman Coulter is recalling Access Total T4 Calibrators because specific lots do not meet their claimed 12-month expiration date.
Radiometer America Inc is recalling Qualicheck 1+ quality control solution due to a barcode error that incorrectly enters a pH control range into blood gas analyzers.