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.
Advanced Food Concepts is recalling GU Energy Chews because testing confirmed the presence of cyclamates, an ingredient not declared on the label.
Howmedica is recalling five custom implant systems because they lacked updated instructions clarifying the locking mechanism and screw warnings.
Advanced Food Concepts is recalling GU Energy Stroopwafels because testing confirmed the product may contain cyclamates, an ingredient not permitted in food.
Advanced Food Concepts is recalling GU Energy Stroopwafels because testing confirmed the presence of cyclamates, an ingredient not declared on the label.
StoneRidge Wholesale Division LLC is recalling approximately 656 pounds of pork and beef bologna products because they contain undeclared sodium nitrite and sodium erythorbate.
Biscomerica, Inc. is recalling Sweet Serenity Caramel Sea Salt Chocolate Chip Cookies because the packaging fails to list milk in the 'contains' statement, despite milk being an ingredient.
Papa John's Salads & Produce is recalling Superfood Salad Kits because peanuts were packed instead of cashews, creating an undeclared allergen hazard.
Roche Diagnostics Hematology is recalling 17 cobas m 511 integrated hematology analyzers due to discrepant results in patients with severe microcytic anemia.
J and J Bunting, Inc. is recalling Kowalski's Markets kalbi rub because it contains wheat, which is not declared on the label.
DePuy Orthopaedics is recalling two lots of CORAIL femoral stems labeled as Size 11 but actually Size 12 due to fit and mechanical risks.
Terumo is recalling Tubing Pack Convenience Kits labeled with an incorrect expiration date of April 30, 2019.
CryoLife, Inc. is recalling BioGlue Spreader Tips because incorrect labels were applied to the packaging, and some required components were missing from the boxes.
OMNIlife science Inc. is recalling 16 units of ApeX-LNK Acetabular Inserts due to improper labeling on internal packaging and patient labels.
Implant Direct Sybron Manufacturing is recalling 124 units of ImplantDirect dental implants because the main vial label lists an incorrect part number, although the cap label is correct.
Nobel Biocare is recalling 74 units of Multi-Unit Abutments because the product labels are missing the lot number, expiration date, and other required information.
Forest River is recalling 2019 Prime Time Crusader fifth-wheel trailers because the Federal Placard lists an incorrect axle weight capacity, which could lead to axle overload and loss of control.
Edwards Lifesciences is recalling one SAPIEN 3 Transcatheter Heart Valve because it was packaged with the incorrect valve size relative to the label.
The Hain Celestial Group is recalling alba BOTANICA sport mineral sunscreen because the wrong product formulation was placed in the packages.
Canadian Hospital Specialties is recalling specific lots of pediatric feeding tubes because they may be packaged with the incorrect length as labeled.
Valeris Medical is recalling 113 Apollo XT Suture Anchors because the labels incorrectly identified the material as titanium instead of PEEK.
Hee Chang Dairy & Food Co., LTD is recalling Black Bean Cereal Latte because FDA inspection found undeclared allergens in the product.
Pinnacle Food Group is recalling Wish Bone House Italian Salad Dressing because some bottles contain undeclared milk and egg.
Roche Diagnostics is recalling the Elecsys Vitamin D total II test system because it may produce falsely elevated, non-reproducible results, potentially leading to incorrect vitamin D dosage adjustments.
Hee Chang Dairy & Food Co. is recalling Citron Tea packets because the citron powder contains undeclared corn syrup and lactose.
Hee Chang Dairy & Food Co., LTD is recalling Black Bean Job's Tears Tea because FDA inspection found undeclared allergens in the product.