Hazard
9,610 recalls in our database tag this hazard, drawn from FDA, USDA FSIS, CPSC, and NHTSA source notices.
Of the 9,610 mis labeling recalls we have scored against our rubric, 161 (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.
Urban Oven, LLC is recalling specific cookie varieties because the label fails to declare milk, a major food allergen, derived from butter.
Ormco is recalling TF Adaptive Gutta Percha Points because the inner label is misidentified as ML3, though the outer package correctly identifies the product as SM3.
Ortho-Clinical Diagnostics is recalling VITROS 350 Chemistry Systems due to increased error codes when using specific calibrators.
Zimmer Biomet is recalling a specific lot of M/L Taper Hip Prostheses because the device was incorrectly etched as 'STD' instead of 'EXT', although the packaging is correct.
Verathon is updating manuals for BladderScan and AortaScan devices to clarify they are not for diagnosing abdominal aortic aneurysms.
Reily Foods is recalling Carroll Shelby White Chicken Chili kits because the label incorrectly stated 0 mg sodium per serving instead of 590 mg.
Ortho-Clinical Diagnostics is recalling VITROS 4600 Chemistry Systems because they may generate specific error codes when used with a recalled Calibrator Kit 9 lot.
Forest River is recalling specific Amera-Lite, Cargo Mate, Continental Cargo, and US Cargo trailers because incorrect tire pressure labels may lead to underinflation and tire failure.
Volcano Corporation is recalling R-100 Sterile Equipment Covers because the outer shipping boxes may display incorrect expiry dates, although the inner product is correctly labeled.
The FDA is recalling 1,010 units of pediatric feeding tubes because 8FR PVC tubes were incorrectly packaged in 6.5FR polyurethane packs.
Aesculap Inc. is recalling 1,232 units of Columbus Revision and EnduRo Knee System packaging labeled as cementless, which are indicated for use with bone cement only.
Scenic Fruit Company is recalling 331 units of Nutrifruit brand Freeze Dried Mango Powder because the label incorrectly lists 625.7 grams of carbohydrates per serving instead of 6 grams.
Medical Action Industries is recalling 180 PICC/CVC Secure Dressing Change kits because the presence of CHG is not identified on the exterior labeling.
Volcano Corporation is recalling certain lots of R-100 Sterile Equipment Covers because the outer shipping boxes may display incorrect expiry dates, although the inner product is correctly labeled.
Scenic Fruit Company is recalling Nutrifruit Freeze Dried Black Raspberry Powder because the label incorrectly states 0 grams of sugar per serving instead of 2 grams.
Frozen Specialties Inc is recalling Hannaford Cheese Crispy Thin Crust Pizza because the packaging displays a Kosher symbol, although the product is not Kosher.
Frozen Specialties Inc is recalling Food Lion microwaveable crispy thin crust pizza because the packaging displays a Kosher symbol that does not represent actual Kosher status.
Frozen Specialties Inc is recalling Food Lion Cheese Crispy Thin Crust Pizza because the packaging displays a Kosher symbol, but the products are not Kosher.
Namias of Arizona is recalling approximately 19,200 pounds of fully cooked chicken products due to misbranding and an undeclared soy allergen.
Philips is recalling IntelliVue Info Center iX software because reconstructed ECG leads may misrepresent waveforms in specific leads.
Philips is recalling PIIC Classic Upgrade patient monitors because reconstructed ECG leads may misrepresent waveforms on the Information Center iX.
Philips is recalling IntelliVue Info Center iX monitors because reconstructed ECG leads may misrepresent waveforms, potentially affecting clinical interpretation.
Stryker is recalling Vitallium Wire because the instructions incorrectly state the non-sterile device is sterile, omitting required sterilization steps.
Fresenius Medical Care is recalling Naturalyte Liquid Acid Concentrate because the label incorrectly lists the calcium concentration.
President East Company is recalling frozen kingfish steaks because FDA analysis found the product was decomposed and actually Spanish mackerel.