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.
ALFA INTERNATIONAL SEAFOOD INC is recalling Full Moon Fish Tuna Steaks because the labels contain incorrect manufacturer numbers, pack dates, and expiration dates.
Becton Dickinson is recalling 75 units of 13 Fr Trialysis Catheters because a portion of the lot was incorrectly packaged with a 12.5cm catheter instead of a 15cm catheter.
Datascope Corp. is recalling seven low level output cables for intra-aortic balloon pumps because they were packaged with incorrect cables.
Productos La Samaritana is recalling specific lots of tomato tortillas because they contain FD&C Red #40, which is not declared on the label.
Epic Enterprises is recalling Dr. Pepper 24-pack cans in Connecticut, Maine, and Rhode Island because they contain undeclared aspartame.
Helena Laboratories is recalling 899 SPIFE Alkaline Hemoglobin Kits because they contain incorrect instruction inserts referencing unavailable electrode parameters.
Productos La Samaritana, Inc. is recalling specific lots of La Samaritana Tortillas because they contain FD&C Red #40, which was not declared on the label.
New Seasons Market LLC is recalling Honey Cake because the packaging lists buttermilk and sour cream but fails to declare milk as an allergen.
Stryker Neurovascular is recalling Synchro2 guidewires because the product labels contain a typographical error in the millimeter dimension for the outer diameter.
Keystone RV Company is recalling 2014 Springdale 253FWRLLS trailers because the Federal Identification Tag may list incorrect tire, rim, and axle sizes, potentially leading to unintentional overloading.
Stryker Neurovascular is recalling Synchro2 guidewires because the product labels contain a typographical error in the millimeter dimension.
Stryker Neurovascular is recalling 305 Synchro2 guidewires because the product labels contain a typographical error in the millimeter dimension.
Stryker Neurovascular is recalling 107 Synchro2 guidewires because the product labels contain a typographical error in the millimeter dimension for the outer diameter.
Stryker Neurovascular is recalling Synchro2 guidewires because the product labels contain a typographical error in the millimeter dimension for the outer diameter.
Arbor Pharmaceuticals is recalling specific lots of Testosterone Cypionate Injection because shipper cartons were mislabeled, potentially causing confusion with different vial sizes.
Stryker Neurovascular is recalling Synchro2 guidewires because the product labels contain a typographical error in the millimeter dimension for the outer diameter.
Sandoz Inc is recalling 76,644 bottles of Gatifloxacin Ophthalmic Solution 0.5% because the package insert is incorrect or missing.
Stryker Neurovascular is recalling Synchro2 guidewires because the product labels contain a typographical error in the millimeter dimension for the outer diameter.
Sandoz Inc. is recalling 346,929 bottles of Neomycin and Polymyxin B Sulfates and Dexamethasone Ophthalmic Suspension due to incorrect or missing package inserts.
Sandoz Inc is recalling Bimatoprost Ophthalmic Solution 0.03% because the package insert is incorrect or missing. The recall covers 346,929 bottles distributed nationwide.
Nephron Pharmaceuticals is recalling 19,390 syringes of Succinylcholine Chloride Injection because of incorrect or missing lot and expiration dates.
Padrino Foods is recalling beef tamales labeled as beef and sirloin that contain pork. The recall affects products sold in Kansas, Louisiana, Oklahoma, and Texas.
New York Style Sausage Co. issued a public health alert for raw pork bangers containing undeclared sesame seed. No illnesses have been reported.
Life Technologies is recalling Torrent Suite Dx software because it may incorrectly display positive results for specific clinical variants.
Life Technologies is recalling Torrent Suite Dx software because it may incorrectly display positive results for clinical variants.