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.
Highland Ridge RV is recalling 84 units of the 2018 Open Range light travel trailer because the Federal Label lists an incorrect Gross Axle Weight Rating.
Crown Candy Corporation is recalling Old Fashioned Pecan Divinity due to intermittent labeling errors that omitted the pecan allergen statement.
Crown Candy Corporation is recalling Old Fashioned Coconut Bon Bons because intermittent labeling errors caused some tubs to be mislabeled with Pecan Divinity ingredients, resulting in an undeclared pecan allergen.
TEI Biosciences is recalling 4,081 units of PriMatrix acellular dermal tissue matrix because some Instructions for Use contained missing or duplicate pages.
DeRoyal is recalling 226 sterile surgical kits because the included povidone iodine prep pads do not support the 36-month expiration date listed on the label.
Stryker Neurovascular is recalling one Trevo XP ProVue System kit because the carton sleeve did not match the physical contents of the pack.
Spineart SA is recalling Tryptik 2 C-Plate self-tapping screws because the product labeling incorrectly displays a sketch of a self-drilling screw.
Spineart SA is recalling 120 units of Tryptik 2 C-Plate Self-Tapping Screws because the product labeling incorrectly displays a sketch of a self-drilling screw.
Spineart SA is recalling 15 units of Tryptik 2 C-Plate Self Tapping Screws because the product labeling incorrectly displays a sketch of a self-drilling screw.
Spineart SA is recalling 9 units of Tryptik 2 C-Plate Self-Tapping Screws because the product labeling displays a sketch of a self-drilling screw instead of the correct self-tapping screw.
Spineart SA is recalling 16 units of Tryptik 2 C-Plate Self Tapping screws distributed in California because the product labeling contains an incorrect sketch of a self-drilling screw.
Spineart SA is recalling 54 units of Tryptik 2 C-Plate self-tapping screws because the product labeling incorrectly displays a sketch of a self-drilling screw.
Spineart SA is recalling 8 units of Tryptik 2 C-Plate Self Tapping screws because the product labeling incorrectly displays a sketch of a self-drilling screw.
Perdue Foods is recalling approximately 530 pounds of chicken breast tenderloin fritters because they contain egg whites, an undeclared allergen.
Café Spice GCT Inc. is recalling ready-to-eat chicken salad products because they contain milk, an undeclared allergen, and are mislabeled as chicken wraps.
Duke Sandwich Productions is recalling approximately 743 pounds of chicken salad products because they were packaged in pimento cheese containers with mismatched labels.
Lovebiotics, LLC is recalling The Coconut Cult Coconut Cream Probiotic Coconut Yogurt because the label lists sodium caseinate but fails to explicitly identify milk as an allergen.
Harrisburg Dairies is recalling 365 brand and Harrisburg Dairies brand Egg Nog because dried egg yolks were not listed in the ingredient statement.
Lovebiotics, LLC is recalling The Coconut Cult Mango Cream Probiotic Coconut Yogurt because the allergen statement lists sodium caseinate but fails to identify milk as the source.
Daisy's Bakery Inc. is recalling Gourmet Concha products because they contain an undeclared milk allergen. The mislabeled items were distributed to five states.
KRS Global Biotechnology is recalling 898 vials of Sincalide 5 mcg due to incorrect or missing lot and expiration dates.
KRS Global Biotechnology is recalling 3,000 Prednisolone 10 mg tablets because the expiration date exceeds the stability of an ingredient.
KRS Global Biotechnology is recalling 235 vials of Trimix #22F because the Beyond Use Date exceeds the expiration date of at least one ingredient.
KRS Global Biotechnology is recalling 129 vials of QUADMIX #18 because the Beyond Use Date exceeds the expiration date of at least one ingredient.
KRS Global Biotechnology is recalling Sermorelin 500 mcg tablets because the expiration date exceeds the shelf life of an ingredient.