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.
Baxter Healthcare is voluntarily recalling one lot of Baxa Vial Adapters due to an incorrect expiry date.
Conagra is recalling Kroger Break 'N Bake Chocolate Chip Cookie Dough because peanut butter was present but not listed on the label.
Dove Chocolate Discoveries is recalling 18 oz boxes of Fruit Collection Dark Chocolate due to mislabeling. The boxes contain Cinnamon Dusted Dark Chocolate Almonds instead of the labeled fruit mix.
Saratoga Therapeutics is recalling ebA Multivitamin tablets because they contain milk components despite labeling stating they are free of milk.
The Warrell Corporation is recalling chocolate covered peanuts mislabeled as raisins because the peanut allergen is not identified on the packaging.
The Seafood Exchange of Florida is recalling H-E-B Jumbo Butterfly Shrimp because the product contains coconut, which is not listed on the label.
Siemens Healthcare Diagnostics is recalling ADVIA Chemistry A1c_3 Calibrators because they cause a positive bias of up to 12% in HbA1c test results.
Greenland Trading Corp is recalling El Basham Apricot Dried Paste because the product does not declare its identity in English. The recall covers 100 cases distributed to five states.
La Terra Fina is recalling one lot of Spinach Artichoke and Parmesan Dip because the label displays the ingredient and nutrition information for Caramelized Onion Dip.
Advance Pharmaceutical Inc. is recalling 16,440 bottles of Enteric Coated Aspirin 81 mg due to a label mix-up where one bottle contained Acetaminophen 500 mg.
See's Candies is recalling Dark Chocolate Blueberries because milk was omitted from the ingredient list. The product was distributed in the US, Hong Kong, and Taiwan.
Whole Foods Market is recalling Sour Cherry Crostata pies because egg wash is used in the product but is not listed on the ingredient list or allergen statement.
Whole Foods Market is recalling Blueberry Crostata pies because egg wash is used in the product but is not listed on the ingredient or allergen statement.
Synthes (USA) Products LLC is recalling 119,891 units of 2.4mm VA-LCP Two Column Volar Distal Radius Plates due to a labeling error in the US Technique guide.
Sarken, Inc. is recalling STAT! Multi-Drug Test Panels because they were distributed without adequate labeling and instructions for use, which could lead to misuse and incorrect test results.
Philips Healthcare is recalling 89 Easy Upgrade DR systems because a mirror icon on images could be misinterpreted as a right lead marker if the image is mirrored in a PACS system.
Ann's House of Nuts is recalling Daily Chef Tropical Fruit & Nut Blend because it contains undeclared Yellow #5 and #6 dyes.
Micro Therapeutics Inc is recalling 62 Pipeline Embolization Devices because the instructions for use are missing specific contraindications regarding pre-existing stents and medication designations.
Synthes USA HQ, Inc. is recalling 11 units of 2.4 mm VA-LCP distal radius plates that may be incorrectly etched with 'R' instead of 'L'.
SpineNet is recalling 400 anterior cervical cages because the instructions for use contained statements that should have been removed prior to marketing.
Sarken, Inc. is recalling STAT! 1-Panel Test Kits because they were distributed without adequate labeling and instructions, which could lead to misuse and incorrect test results.
Sarken, Inc. is recalling SARKEN STAT! 1-Panel Test Kits-THC because they were distributed without adequate labeling and instructions, which could lead to misuse and incorrect results.
Nidek Inc is recalling NAVIS-EX software because left eye images may be incorrectly saved as right eye images.
Sarken, Inc. is recalling STAT! 1-Panel Test Kits because they were distributed without adequate labeling and instructions, which could lead to misuse and incorrect test results.
Sarken, Inc. is recalling STAT! 1-Panel Test Kits because they were distributed without adequate labeling and instructions, which could lead to misuse and incorrect results.