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.
E3 Artisan is recalling 40 bars of 3-piece Blood Orange Meltaways because FDA samples tested positive for undeclared milk.
E3 Artisan is recalling specific dark chocolate bars because FDA testing found undeclared milk on the labels.
E3 Artisan is recalling 636 dark chocolate bars because FDA testing found undeclared milk, a major food allergen, in the product.
Zingerman's Candy Manufactory is recalling 8-ounce bags of Chocolate Marshmallows because they contain undeclared soy. The recall affects 134 units distributed across 18 states and Washington, D.C.
Hain Celestial is recalling Roastaroma Herbal Tea because some packages are labeled 'Gluten Free' but contain barley.
Zimmer Dental Inc. is recalling specific Trabecular Metal dental implants because safety information was missing from the instructions for use.
Zimmer Dental Inc. is recalling specific Trabecular Metal dental implants because safety information was omitted from the instructions for use.
Pharmacaribe LLC is recalling PulmoSal 7% Sodium Chloride inhalation solution because vials were labeled as USP 7% Hypertonic saline instead of PulmoSal 7% (pH+).
Zimmer Dental Inc. is recalling specific Trabecular Metal dental implants because safety information was omitted from the latest instructions for use.
Bard Peripheral Vascular Inc is recalling four units of Bard Distaflo Vascular Bypass Grafts due to size mislabeling. The 8 mm grafts are incorrectly labeled as 6 mm.
Zimmer Dental Inc. is recalling specific dental implants because the latest instructions omitted information for certain models.
Zimmer Dental Inc. is recalling specific Trabecular Metal implants because safety information was omitted from the instructions for use.
Zimmer Dental Inc is recalling specific dental implants because the instructions for use omitted safety information regarding the 3.7 mmD and 4.1 mmD Trabecular Metal models.
Bard Peripheral Vascular Inc is recalling four units of the Bard Distaflo Vascular Bypass Graft because the product is mislabeled as 6 mm when it is actually 8 mm.
Zimmer Dental Inc is recalling specific Trabecular Metal dental implants because safety information was omitted from the instructions for use.
Zimmer Dental Inc is recalling specific dental implants because safety information was omitted from the instructions for use.
Taylor Farms Pacific is recalling Signature Cafe Traditional Stuffing because the label fails to declare soy, milk, and wheat.
This Bar Saves Lives is recalling This Kid Saves Lives Chocolate Chip bars because they contain whey protein but do not identify milk on the label.
Philips is recalling INTEGRIS and Allura medical imaging systems because a software issue may cause still images to be mistaken for live images.
Philips is recalling Allura Xper FD10 systems because a software defect may cause still images to be mistaken for live images during cardiovascular procedures.
Philips is recalling 13,297 Allura Xper FD20/10 systems because a software error may cause still images to be interpreted as live images.
Philips is recalling UNIQ and Allura systems because a software issue may cause still images to be misinterpreted as live images during medical procedures.
Philips is recalling INTEGRIS Allura X-ray systems because a software error may cause still images to be displayed as live images, potentially leading to misinterpretation.
Radiometer America Inc is recalling 375 AQURE Systems (Model 933-599) because a design error may leave the sample type field blank, potentially leading to misinterpretation of blood gas and immunoassay results.
Philips is recalling Allura Centron systems because a software error may cause still images to be misinterpreted as live images during medical procedures.