Hazard
9,611 recalls in our database tag this hazard, drawn from FDA, USDA FSIS, CPSC, and NHTSA source notices.
Of the 9,611 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 589 (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.
StoneRidge Wholesale Division LLC is recalling pork tenderloin products because they contain undeclared milk, a known allergen.
Real Foods of Seattle is recalling strawberry trays with Devonshire dip due to the addition of an incorrect dressing containing undeclared egg and soy.
Abbott Laboratories is recalling Similac Advance infant formula because export-bound product with Chinese labeling was distributed in the US.
Southern Implants, Inc. is recalling 130 units of MAX-TL and Z-MAX dental implants because the labeled packages contained the wrong implant type.
Keystone Food Products Inc. is recalling specific brands of veggie chips because the sodium content on the label is incorrect. The product contains approximately 290 mg of sodium per serving, not the 55 mg claimed.
Keystone Food Products is recalling specific brands of veggie sticks and straws because the sodium content listed on the label is incorrect.
Richard-Allan Scientific is recalling 132 gallons of CYTO-STAIN R Stain because the bottles were incorrectly labeled as CYTO-STAIN G, although the contents are correct.
Bear Creek Smokehouse is recalling approximately 3,700 pounds of beef products because they contain soy, a known allergen not declared on the label.
L & L Foods is recalling 30,665 pounds of bacon bits because the product contains soy lecithin, an allergen not listed on the label.
Sole Grano LLC is recalling Fairway Organic Cranberry Low Fat Granola because it may contain undeclared almond and wheat allergens.
T. Marzetti Company is recalling LaRosa's Italian Dressing packets because the ingredient labels were switched, potentially leaving undeclared milk, egg, or sulfite allergens.
MegaMex Foods is recalling Herdez Chilpotle Peppers due to an undeclared wheat allergen. The recall covers 58,749 cases distributed nationwide.
T. Marzetti Company is recalling LaRosa's Creamy Garlic Dressing packets because ingredient labels were switched, resulting in undeclared milk, egg, and sulfites.
CooperSurgical is recalling 95 units of Pessary Kit-CUBE#2 because the packaging label displays the incorrect size.
Baxter Healthcare is recalling 55 AMIA v1.0 APD Systems to add a warning about the risk of unintended increased intraperitoneal volume for vulnerable patients.
Baxter is recalling Self-Righting Syringe Tip Caps because the latex symbol is missing from the labels.
Arjo Hospital Equipment AB is recalling 226 Rotoprone Therapy Systems because their labeling and instructions for use contain unapproved medical claims.
Arrow International Inc. is recalling 165 units of FiberOptix Intra-Aortic Balloon Catheter Kits because the outer package label incorrectly identifies the product size.
Arjo Hospital Equipment AB is recalling 271 RotoRest Delta Advanced Therapy Systems because their labeling contains unapproved medical claims.
Arjo Hospital Equipment AB is recalling 567 TriaDyne Proventa Critical Care Therapy Systems because their labeling and instructions for use contain unapproved medical claims.
Nanophase Technologies is recalling 4,104 cartons of Z-COTE HP 1 Transparent Zinc Oxide powder due to illegible labels where writing is rubbing off.
PACCAR is recalling 2006-2016 Peterbilt trucks because tire labels may list incorrect pressure, risking tire failure and crashes.
Forest River is recalling 2015 Wildcat fifth-wheel trailers because incorrect weight labels may lead to overloading and trailer pin box failure.
Angiodynamics is recalling 43 Starburst MRI Semi-Flex Electrode Devices because a printed distance mark is incorrectly located 4cm from the tip instead of 5cm.
Medtronic is recalling specific neurostimulator models because enabling cycling at certain settings may decrease battery life and cause inaccurate longevity estimates on the programmer.