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.
Forest River is recalling certain 2022 Cherokee toy haulers because the Tire and Loading Information placard may show incorrect rim specifications, potentially causing improper tire installation and crash risk.
Sandridge Food Corporation is recalling Macaroni & Cheese (Macarrones con Queso) distributed to restaurants and a hotel in Texas because the product contains egg but does not declare this allergen on the label.
Tapemark's iontoPATCH On-the-Go patches contain incorrect dosage information printed on the pouch label, though the primary carton label is correct. Approximately 5,141 cartons were distributed nationwide.
Keurig Dr Pepper is recalling Diet Snapple Peach Tea 16 oz bottles with expiration date February 5, 2022, because some units labeled as diet and zero sugar may contain sugar due to a production error.
Kettle River Products is recalling approximately 1,464 pounds of chicken alfredo pizza due to misbranding and an undeclared wheat allergen. No adverse reactions have been reported.
BUBS Naturals Fountain of Youth Formula collagen supplement is recalled nationwide because it contains undeclared milk from an MCT oil powder ingredient. Consumers with milk allergies or sensitivities should not consume this product.
Denver Solutions, LLC (doing business as Leiters Health) is recalling Moxifloxacin 1 mg/mL intracameral injection solution because vials labeled as 1 mg/mL may actually contain 5 mg/mL, creating a serious dosing error risk.
Cesarina Bakery is recalling Cesarina Sesame Seed Cookies (16 oz) because they contain undeclared milk, which may pose a risk to consumers with milk allergies.
Cesarina Bakery, Inc. is recalling Cesarina Cookies (Assorted, 16 oz) due to undeclared milk. Consumers with milk allergies face a potential allergic reaction risk.
Maquet Cardiovascular is recalling Hemashield Gold vascular grafts due to probable mislabeling. A different graft product may have been packaged in the carton.
Cesarina Bakery, Inc. is recalling Cesarina Cookies, Fiochetto, Apricot Raspberry Guava (16oz boxes) because they contain undeclared milk, a common allergen. The recall affects domestic distribution and applies to multiple lot codes with expiration dates ranging from March 2022 through May 2022.
San Mar Manufacturing Corporation is recalling Hacienda Las Glorias Premium Bebida de Parcha (Passion Fruit Drink) 16 oz. bottles due to undeclared Yellow #5 dye. The product was distributed domestically only.
Cesarina Bakery is recalling Flora Raspberry Sandwich Pastries because they contain undeclared milk, which poses a risk to consumers with milk allergies. The recall affects 1,028 cases distributed domestically.
Cesarina Bakery, Inc. is recalling Cesarina Cookies Tutti Frutti (16 oz) because the product contains undeclared milk, a common allergen not listed on the label.
Medtronic is recalling Astra XT DR patient identification cards that were printed with an incorrect statement about MR safety conditional status. The erroneous cards were distributed in the US, Canada, and Northern Mariana Islands.
Medtronic is recalling 187 Medical Device Identification Cards for Sprint Quattro Lead implants printed with an erroneous statement about MR conditional system status. Affected cards were distributed in the US, Canada, and Northern Mariana Islands.
Morton Iodized Salt labeled as iodized actually contains salt without iodine fortification. The recall affects 16,920 canisters distributed to retailers in Colorado and California.
USDA FSIS issued a public health alert for Trader Ming's frozen wonton soup containing undeclared shrimp and pork. Consumers with allergies should not consume the product.
ELLENOS Real Greek Yogurt in Mango flavor is recalled because the product contains egg but the label does not declare it. The recall affects 3,912 units distributed in Oregon and Washington.
Boston Scientific AUTOLITH TOUCH Bipolar Electrohydraulic Lithotripter devices distributed to Massachusetts have reversed high and low power settings in Russian, Romanian, Slovak, and Czech language versions. Users selecting a power level may receive the opposite setting.
Trail Toddy & Company LLC is recalling Spiced Irish Coffee Hint of Cocoa packets because milk is not declared on the label despite cream powder being present in the product. The product was distributed in Illinois, Montana, and Massachusetts.
Wright Medical Technology is recalling INBONE Total Ankle System implants because the package contents and package labeling do not match.
Keurig Dr Pepper is recalling 7UP Zero Sugar Lemon Lime Soda due to unlabeled sulfites detected after customer complaints about off flavor and aroma. The recall affects 9,152 cases distributed nationwide.
Keurig Dr Pepper is recalling Polar Black Cherry Premium Seltzer 12-packs due to unlabeled sulfites. The recall affects 7,849 cases distributed nationwide with product code date 12/16/2022.
Wright Medical Technology is recalling the INBONE Total Ankle System because package contents do not match the package labeling on affected units distributed in Michigan and Pennsylvania.