Hazard
9,606 recalls in our database tag this hazard, drawn from FDA, USDA FSIS, CPSC, and NHTSA source notices.
Of the 9,606 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.
Lifetime Brands has recalled about 2,700 hot chocolate pots sold at Williams-Sonoma because they are mislabeled as microwave safe. If microwaved, the metallic paint can spark and cause a fire.
Pietrzyk Foods is recalling The Holy Gouda Pierogi due to undeclared soy lecithin. Consumers with soy allergies should not consume this product.
Meijer is recalling 1,590 tubs of True Goodness Yogurt Alternative because the product contains almond but is mislabeled as oat-based. This poses a risk to consumers with tree nut allergies.
Hippos and Hashbrowns is recalling Take & Bake Everything Biscuits due to missing allergen labeling for milk and wheat. The product label does not include the common names for these allergens.
RED SUN TARO FLAVOR POWDER is recalled due to undeclared milk (sodium caseinate) and incorrect color additive labeling. The product was distributed in Iowa and may pose a risk to consumers with milk allergies.
Hippos and Hashbrowns is recalling Take & Bake Maple Pecan Biscuits sold in Texas because the product labels fail to declare milk and wheat allergens. Consumers with allergies should not consume this product.
Forest River is recalling 2022 East to West Entrada 24FM motorhomes because the certification label incorrectly lists 6 belted seating positions instead of 4.
Power Life High Impact Plant Protein in chocolate flavor is recalled because the product label does not declare milk as an ingredient, creating a serious allergic reaction risk for milk-allergic consumers.
Cranberry Sweets & More Inc is recalling Peanut Butter Meltaway chocolates mislabeled as Mint Meltaways. The product contains undeclared peanut, a major food allergen, posing risk to allergic consumers.
Hikma Pharmaceuticals recalled Ganciclovir for Injection due to a labeling error where one vial per carton was mislabeled as Cladribine Injection, creating a risk of incorrect medication administration.
Wismettac Asian Foods is recalling Premium Quality Shirakiku Fish Sausage Jalapeno because the casing contains undeclared bovine collagen. The product was distributed across 23 U.S. states.
Corin Ltd is recalling BIOLOX DELTA ceramic hip replacement heads because some units are labeled with incorrect sizes. The recall affects 12 units distributed in seven U.S. states.
Corin Ltd is recalling BIOLOX Delta Ceramic Hip Implant Heads nationwide due to size labeling errors. The 36XL size is labeled as 32XL and vice versa, which could result in implantation of an incorrectly sized component.
BayCare Integrated Service Center is recalling 250 iohexol injection syringes mislabeled as 300 mg iodine/mL but actually containing 350 mg iodine/mL. The labeling error could result in dosing mistakes.
SUBURBAN BREAD CO. is recalling Big Sky Chocolate Chunk Granola (14oz pouches) because product labeling fails to declare milk, a sub-ingredient present in the granola. This poses a risk to consumers with milk allergies.
Big Sky Chocolate Chunk Peanut Butter Chip Granola (14oz) is being recalled because the product labeling fails to disclose milk allergen in its sub-ingredients. Consumers with milk allergies should not consume this product.
Carefusion is recalling bipolar forceps due to incomplete Instructions for Use. The IFU is missing content about power supply interface and cleaning procedures.
Medical Action Industries is recalling Port Access Kits that are incorrectly labeled as IV Start Kits on the individual kit label. The case label is correct; mislabeling could cause confusion about the product's identity.
CareFusion bipolar forceps recalled due to missing instructions on power supply interface and cleaning/maintenance procedures. Corrected documentation is now available.
Carefusion recalls bipolar forceps due to incomplete Instructions for Use missing power supply interface and maintenance guidance. No injuries reported.
Volkswagen Group of America is recalling 2023 Audi S3, RS3, and A3 vehicles because the B-pillar safety label is missing weight capacity information.
Cytocell Ltd. recalls CytoCell BCL11B Proximal probe used in T-cell malignancy testing (lot RD22/230/10). The package insert contains an incorrect chromosome map that doesn't match the probe design.
Southmedic is recalling 450 units of sterile surgical blade cartridges (Lot W92761) because the product was not sterilized but was labeled and distributed as sterile. Non-sterile surgical blades could cause infection if used on patients.
Acella Pharmaceuticals is recalling Phenytoin Sodium Injection due to missing barcodes on vial labels. The recall affects 574 cartons distributed nationwide.
Acella Pharmaceuticals is recalling Phenytoin Sodium Injection because the primary vial label is missing a barcode. The recall affects 637 cartons distributed nationwide.