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.
Dolcetta Artisan Sweets is recalling Maple-Pepper Caramels because they contain undeclared soy lecithin and milk. The product was distributed in Oregon and Washington.
Dolcetta Artisan Sweets is recalling 98 boxes of Espresso Caramels sold in Oregon and Washington due to undeclared soy lecithin.
Dolcetta Artisan Sweets is recalling Peanut Crisp Truffles because the product contains undeclared soy lecithin, a potential allergen.
Companion Foods Corp. is recalling Braised Bamboo Shoot Tips with Chili because an FDA inspection found wheat was not properly declared in the ingredient list.
Gerber is recalling Pasta Pick-Ups Cheese Ravioli because the egg allergen is missing from the 'Contains' statement on the packaging.
ConMed is recalling sterile handpiece sheaths that were packaged in error with non-sterile units. The mislabeling could lead to the use of non-sterile sheaths.
ConMed is recalling Hyfrecator 2000 accessory packages because they contained non-sterile handpiece sheaths labeled as sterile.
ConMed is recalling Hyfrecator 2000 ESU cartons because they were packaged with non-sterile handpiece sheaths labeled as sterile, posing a risk of infection.
Companion Foods Corp. is recalling Braised Bean Curd (Mock Chicken) because wheat is not properly declared as a sub-ingredient in the ingredient list.
Dolcetta Artisan Sweets is recalling 250 Rosemary Caramel Bars in Oregon and Washington due to undeclared soy lecithin.
Dolcetta Artisan Sweets is recalling Peppermint Caramel Truffles because the product contains undeclared soy lecithin and milk. The recall affects 100 boxes distributed in Oregon and Washington.
Dolcetta Artisan Sweets is recalling 300 Dark Chocolate Coconut Bars distributed in Oregon and Washington due to undeclared soy lecithin and milk.
ConMed is recalling Hyfrecator 2000 handpiece sheaths because non-sterile units were packaged in pouches labeled as sterile, posing a risk of infection.
Companion Foods Corp. is recalling Vegetarian Minced Meat with Shiitake because an FDA inspection found wheat was not properly declared in the ingredient list.
Companion Foods Corp. is recalling Szechuan Style Kung-Pao Sauce because wheat is not properly declared in the ingredient list, posing a risk to individuals with wheat allergies.
Companion Foods Corp. is recalling Braised Bamboo Shoot Tips because wheat is not properly declared in the ingredient list.
Companion Foods Corp. is recalling Vegetarian Tuna Fish cans because an FDA inspection found wheat was not properly declared in the ingredient list.
Cardiovascular Systems Inc. is recalling one lot of ViperWire Advance Peripheral Guide Wires because they may contain the wrong size product.
2k Innovations is recalling Volt Resistance Heated Slippers because FDA inspections found the company made unapproved therapy and medical claims on product information and its website.
Companion Foods Corp. is recalling Fat-Choy Style Vegetable Soup because an FDA inspection found wheat was not properly declared in the ingredient list, despite being listed in the Contains statement.
2k Innovations Inc. is recalling Volt Resistance Heated Therapy Knee Wraps because FDA inspections found the product makes unapproved therapy and medical claims.
2k Innovations Inc. is recalling Volt Resistance Frostie Heated Gloves because FDA inspections found the firm made unapproved therapy and medical claims on product information and its website.
Boston Scientific is recalling Imager II Angiographic Catheters because some packages are mislabeled as Contra 2 curve catheters when they contain Contra curve catheters.
2k Innovations Inc. is recalling Volt Resistance Heated Slippers because FDA inspections found the product makes unapproved therapy and medical claims.
Citron Pharma LLC is recalling 420 bottles of Penicillin V Potassium 500 mg tablets because Amoxicillin 500 mg tablets were found in the bottles.