Hazard
9,610 recalls in our database tag this hazard, drawn from FDA, USDA FSIS, CPSC, and NHTSA source notices.
Of the 9,610 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 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.
President East Company is recalling frozen kingfish steaks because FDA analysis found the product was decomposed and actually Spanish mackerel.
Medtronic is recalling Specify 5-6-5 and 2x8 spinal cord stimulation leads because the labeling does not adequately distinguish between permanent implant and trialing use.
Stryker is recalling Vitallium Wire because the instructions incorrectly state the non-sterile device is sterile, omitting required sterilization steps.
EKOS Corporation is recalling 10 units of the EkoSonic Endovascular System because the device is labeled with a 135 cm working length, but the actual working length is 106 cm.
Becton, Dickinson and Company is recalling 78 units of BD FMC7 FITC reagent because the vial labels display an incorrect expiration date.
Hospira is recalling 10,778 bags of Normosol-M and 5% Dextrose Injection due to an incorrect expiration date printed on the primary container.
Isomeric Pharmacy Solution, LLC is recalling 114 vials of Triamcinolone Diacetate Injectable Suspension because some vials may have incorrect lot numbers or expiration dates.
American Grease Stick Company is recalling Carquest DOT5 Silicone Brake Fluid bottles manufactured between October 2013 and September 2015 due to missing or unclear labeling required by federal safety standards.
Hospira is recalling 213,600 bags of Magnesium Sulfate in Water for Injection because the primary bag labeling may be mislabeled with a barcode that scans as heparin sodium.
Medisca Inc is recalling L-Citrulline API bottles because FDA testing found the product contained N-acetyl-leucine instead of the labeled ingredient.
Medline Industries is recalling 500 mg acetaminophen tablets mislabeled as 325 mg. Consumers should stop using the product and return it to the retailer.
Medline Industries is recalling 325 mg acetaminophen tablets that are actually 500 mg due to a labeling error.
Isuzu is recalling certain 2016 NPR-HD, NPR-XD, NQR, and NRR trucks because typographical errors on the certification label may prevent accurate vehicle loading and maintenance.
Verathon is recalling GlideScope and AVL video laryngoscope reusable blades to update the Operations and Maintenance Manual regarding chemical cleaning cycle limits.
Exactech is recalling 19 Acapella One Interbody Fusion Devices due to incorrect external and internal packaging labels.
JNC International Inc. is recalling Little Temptations Sour Strawberries because they contain undeclared FD&C Blue #1 and Yellow #5.
Sorin Group USA is recalling 60 units of Dual Stage Venous Return Catheters because the cases contained incorrect Instructions For Use (IFU).
Ajinomoto Windsor Inc. is recalling approximately 6,000 pounds of Shirakiku Gyoza Dumplings labeled as beef but containing undeclared pork.
Highland Ridge RV is recalling 2015-2016 travel and fifth wheel trailers because incorrect Gross Vehicle Weight Rating labels may allow overloading, increasing the risk of tire failure and crashes.
Daimler Vans USA is recalling 2015-2016 Sprinter vans because tire pressure labels list incorrect maximum load capacities, which could lead to axle or tire failure.
Forest River is recalling 2016 Coachmen Galleria motorhomes because the Federal Placards incorrectly list seatbelts and omit the Gross Vehicle Weight Rating, increasing crash risk.
E3 Artisan is recalling dark chocolate bars with strawberries, rose petals, and pink peppercorns because FDA samples tested positive for undeclared milk.
E3 Artisan is recalling Meltaways dark chocolate bars because FDA testing found undeclared milk. Consumers with allergies should not consume the product.
E3 Artisan is recalling Meltaway bars because FDA samples tested positive for undeclared milk, posing a risk to consumers with milk allergies.
E3 Artisan is recalling Meltaway bars because FDA testing found undeclared milk, a major allergen, in the product.