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.
Kerry, Inc. is recalling DaVinci Gourmet Classic Caramel Flavored Sauce because an incorrect label failed to declare milk as an ingredient.
Implant Direct Sybron Manufacturing LLC is recalling 11 dental implant units because the vial and cap colors did not match the implant size, potentially causing surgical delays or infection risks.
Ready Pac Foods is recalling Spinach Dijon Salad because the label fails to declare eggs and wheat.
Nextremity Solutions is recalling 40 Stratum Lapidus Plate units because the package labeling indicates a right plate, but the product contains a left plate.
GSK is recalling Theraflu Cough Relief packets because the label lacks a warning for people on sodium-restricted diets.
Morton Salt Inc. is recalling 26 oz canisters of iodized salt that were incorrectly labeled as plain salt, resulting in undeclared dextrose and potassium iodide.
Prollenium Medical Technologies is recalling 48,457 kits of Revanesse Versa because the product is labeled with an 18-month expiration date, but it is only approved for 12 months.
Taewoong Medical Co., Ltd. is recalling 178 esophageal stents because the Instructions for Use (IFUs) shipped with the devices were misprinted.
LivaNova USA Inc. is recalling five Sorin Connect Datapad devices because they have incorrect manufacturing date labels. The devices were distributed in New Jersey and California.
Par Pharmaceutical is recalling 9,936 cartons of Frovatriptan Succinate Tablets, 2.5mg, because they are labeled with an incorrect expiration date.
Merical, LLC is recalling Meijer Joint Health Glucosamine tablets because the label fails to identify crustacean shellfish as an ingredient.
Tres Coronas Bakery is recalling Red Apple and Tres Coronas brand flour tortillas sold in Oregon due to undeclared wheat.
Clinical Diagnostic Solutions is recalling Medonic M-Series Hematology Analyzers due to a risk of sample misidentification and operator injury from exposed needles.
Merical, LLC is recalling Meijer Joint Health Movement Advanced Dietary Supplement because the label fails to declare crustacean shellfish as an allergen.
PediaLift LLC is recalling 11 PediaLift Access Devices because the firm could not obtain a satisfactory Certificate of Conformance from the original vendor regarding labeling requirements.
Microbiologics Inc is recalling 9 units of the Vaginal Verification Panel Lot 8208-11 because Pool 2 contains the wrong organism, Candida krusei.
Wright Medical Technology is recalling two lots of EVOLVE Modular Radial Heads because the product size in the package may be incorrect. Both labels and laser markings are wrong.
Implant Direct Sybron is recalling 72 Legacy 3 dental implants because some packages contain incorrect implants, which could lead to surgery rescheduling.
Zimmer Biomet is recalling 133 Jamshidi Bone Marrow Aspiration Needles because the outer expiration date may exceed the inner label date.
Wright Medical Technology is recalling 39 EVOLVE Modular Radial Heads because the product size inside the package does not match the label or laser marking.
Jjgc Industria E Comercio De Materials Dentarios Sa is recalling two Neodent Tapered Guided Surgery Drills because the laser engraving incorrectly identifies the model.
Randox Laboratories is recalling Liquid Clinical Chemistry Control lot 1021 UE due to a transcription error in the Lipase value.
Honda is recalling 2020 Pilot and Passport vehicles because the certification label ink may wipe away, removing weight rating information and increasing crash risk.
Kindroot LLC is recalling Peach Blossom plant lozenges because the label failed to list fish as the source of collagen peptides.
Custom Healthcare Systems is recalling 240 inpatient dialysis kits because a component contains latex that was not listed on the product labels.