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.
Kettle Foods is recalling Honey Roast Nuts and Fruit Trail Mix because it was made with dried pineapple containing sulfur dioxide instead of untreated pineapple.
Cooper Surgical is recalling 31 units of Incontinence Dish Folding Pessaries because the outer packaging may not reflect the actual product size.
Cooper Surgical is recalling 45 units of Incontinence Dish pessaries because the outer package may not reflect the actual product size.
Cooper Surgical is recalling 20 units of Cube Pessaries because the outer packaging may not reflect the actual product size.
Cooper Surgical is recalling Incontinence Dish Folding Pessaries because the outer package may not reflect the actual product size.
Dymatize Nutrition XPAND Post Xtreme Mass Recovery System is being recalled because the label declares whey but fails to declare milk.
Dymatize Enterprises is recalling specific lots of XPAND Post Xtreme Mass Recovery System because the label declares whey but fails to declare milk.
Dymatize Enterprises is recalling specific lots of XPAND Post Xtreme Mass Recovery System Fruit Punch because the label declares whey but fails to declare milk.
Ron's Pizza Warehouse is recalling approximately 700 pizza dough shells in Ohio because the product contains wheat but lacks allergen labeling.
Alphatec Spine is recalling 7 ILLICO spinal rods that were laser-etched as 110mm but are actually 100mm long.
Keystone Dental Inc is recalling 120 units of PrimaConnex Tapered Implants because the included cover screw was a WD type instead of the labeled SD type.
Beckman Coulter is recalling Creatinine reagents to provide updated instructions for calibration stability and quality control frequency.
Stryker is recalling four units of Specialty Triathlon Knee Sizer Adjustment Housings because the standard femoral stylus does not fit and the left/right markings on the right sizer are reversed.
Synthes USA is recalling four Variable Angle Locking Compression Plates that were incorrectly etched with the wrong part number.
Agfa Corp. is recalling 17 X-ray image plates shipped with incorrect size barcodes, affecting facilities in 10 US states.
Novartis Consumer Health is recalling Nupercainal Ointment because lot numbers and expiration dates may be illegible or missing.
West-ward Pharmaceutical Corp. is recalling 1,763 bottles of Carisoprodol Tablets, 350 mg, because they lack the required C-IV imprint on the label.
Volk Optical Inc is recalling 40 units of 20 Diopter Binocular Indirect Ophthalmoscope lenses due to mixed-up lot number engravings on the devices and packaging.
Novartis Consumer Health is recalling 4 Way Saline Moisturizing Mist bottles because lot numbers or expiration dates may be illegible or missing.
Novartis Consumer Health is recalling Myoflex Pain Relieving Cream because lot numbers and expiration dates may be illegible. The recall covers 2-oz and 4-oz tubes distributed nationwide and in Panama.
Novartis Consumer Health is recalling 4 way Nasal Decongestant Menthol Nasal Spray because lot numbers and expiration dates may be illegible.
Novartis Consumer Health is recalling 4 Way Nasal Spray because lot numbers and expiration dates may be illegible.
Intio Inc. is recalling seven copies of the ClearStart-SVM User Manual due to an editing mistake that could be interpreted as promoting an unapproved use.
See's Candies is recalling 1.7 oz Divinity Easter Eggs with Walnuts because they may contain peanut butter instead of walnuts.
Bay Valley Foods is voluntarily recalling approximately 430,227 cases of boxed pasta mix products because the labeling did not include soy lecithin in the ingredient statement.