Hazard
1,381 recalls in our database tag this hazard, drawn from FDA, USDA FSIS, CPSC, and NHTSA source notices.
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.
Tiffin is recalling certain 2026–2027 recreational vehicles because the Cargo Carrying Capacity label may have been incorrectly printed on white, making it difficult to locate loading and tire pressure information.
Tesla is recalling certain 2025 and 2026 Model Y vehicles because the certification label may not have been installed. Missing weight information on the label could lead to vehicle overloading and increase crash risk.
Jayco is recalling 2025-2026 Entegra Condor and Jayco Granite Ridge motorhomes because their certification labels may have front and rear axle information reversed, potentially leading to incorrect tire pressure and increased crash risk.
General Motors is recalling 2025 Cadillac Lyriq vehicles for inaccurate owner's manual descriptions of rear head restraints. Incorrect manual information may lead to improper adjustment and increased crash injury risk.
Altec is recalling certain 2023-2026 service vehicles because their certification labels show incorrect tire pressure ratings, which could lead to underinflated tires and blowouts.
Forest River is recalling certain 2023 Aurora travel trailers due to an incorrect Gross Vehicle Weight Rating (GVWR) on the Federal placard. The mislabeled weight rating could lead to vehicle overloading and increased crash risk.
Crestline Pharmaceuticals is recalling two lots of warfarin sodium tablets after a labeling error swapped 2.5 mg and 5 mg strengths.
GreenGrow has recalled 11,200 bottles of an herbicide concentrate after labeling errors omitted dilution instructions.
Certain 2025 Nissan Kicks vehicles have certification labels with incorrect Gross Vehicle Weight Rating and Gross Axle Weight Rating values, which could lead to vehicle overloading and crash risk. Some SR trim vehicles with an optional 19-inch wheel package also have incorrect tire size information.
Medline medical convenience kits are being recalled because the outer carton is mislabeled. The packaging states the contents are 1 mL Luer Lock Tuberculin Syringes, but the actual syringes inside are U-100 insulin syringes.
Medtronic is recalling Pocket Adaptor Kits for deep brain stimulation devices due to incorrect Use-By-Dates on product labels. The recall affects 31 units distributed worldwide.
Safecor Health, LLC is recalling Atomoxetine HCl 10 mg capsules because some units are incorrectly labeled as 10 mg when they actually contain 25 mg. Patients taking the mislabeled product may receive an incorrect dose.
Liquid Blenz Soursop Bitters 16 oz and 32 oz bottles may be under-processed, allowing Clostridium botulinum to grow. The product also lists unauthorized health claims. Consumers should not consume and should return bottles.
LIQUID BLENZ CORP is recalling Blackseed Bitters bottles due to potential under-processing that may allow Clostridium botulinum growth. The recall affects 18,190 bottles distributed in New York and online.
Golden State Medical Supply Inc. is recalling Primidone 250 mg tablets due to cross-contamination with trace amounts of Acemetacin API. The affected lots are distributed nationwide.
French Broad Chocolate bonbons are recalled due to mislabeling of walnut content on the printed tasting guide. Consumers with nut allergies relying on the guide could accidentally consume a walnut-containing bonbon.
Loard's Burgundy Cherry Ice Cream 32 oz is recalled for containing undeclared milk and food color additives (Red #40, Blue #1, Blue #2). Consumers with milk allergies should not consume this product.
Silver Moon LP is recalling Loard's Strawberry Ice Cream (32 oz and 56 oz) distributed in Northern California due to undeclared milk and Red #40. The product poses a risk to consumers with milk allergies.
Katalyst Surgical, LLC is issuing a Field Safety Corrective Action for instructions for use (IFU) related to DEX Ophthalmic Tissue Forceps (Model DVF4005-23). The corrective action addresses a labeling issue in the product instructions.
Katalyst Surgical is correcting the instructions for use (IFU) for DEX Ophthalmic Tissue Forceps (Model DVF4019-27) and related scissors due to a field safety issue.
Katalyst Surgical is issuing a Field Safety Corrective Action for 670 units of DEX Ophthalmic Tissue Forceps (Model DVF4019-25) due to updates required in the instructions for use. The device was distributed worldwide.
Katalyst Surgical is issuing a field safety corrective action for DEX Ophthalmic Tissue Forceps (Model DVF4019-25-S) due to instructions for use updates. The recall affects 645 units distributed nationwide in the US and internationally.
XZL Jelly Snacks (12.68 oz bags, 100 cases) distributed to New York and Rhode Island are being recalled because they contain undeclared FD&C Yellow #5, Yellow #6, and Red #40 food coloring additives.
Banana Ice Cream products sold in Northern California under four labels are being recalled due to undeclared Yellow #5 dye. The FDA-classified voluntary recall affects 664 units.
Katalyst Surgical, LLC is correcting instructions for DEX Ophthalmic Tissue Forceps, Model DVF4034-25. The company has issued a field safety corrective action for the product's instructions for use.