Hazard
9,611 recalls in our database tag this hazard, drawn from FDA, USDA FSIS, CPSC, and NHTSA source notices.
Of the 9,611 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 589 (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.
Emparedados Boricua is recalling Tripleta sandwiches in Puerto Rico due to undeclared soy from the cheese ingredient.
Arrow International Inc. is recalling Arrowgard Blue and Blue Plus catheters because the packaging incorrectly lists an echogenic needle, which may not be present.
Fujifilm Medical System USA is recalling 14 MXR-35 Diagnostic X-ray High Voltage Generators because the labeling did not include the certification statement required by 21 CFR Part 10 10.2.
J. R. Simplot is recalling Southwestern Veggies breakfast bowls because an undeclared ingredient, sodium benzoate, was accidentally added to the salsa.
Oasis Medical Inc. is recalling 10,549 bottles of Oasis Tears Lubricant Eye Drops because the label on the immediate bottle is missing.
Flawless Beauty LLC is recalling Tatiomax powder for injection vials because the product was marketed without an approved New Drug Application (NDA) or Abbreviated New Drug Application (ANDA).
Flawless Beauty LLC is recalling Saluta (reduced glutathione) Powder for Injection because it was marketed without an approved NDA/ANDA and is labeled for use as an antidote.
Flawless Beauty LLC is recalling Vitamin C Injection ampoules marketed without an approved NDA/ANDA. The product is sold over the counter with labeling indicating disease treatment.
Kroger is recalling Private Selection Caramel Hazelnut Fudge Truffle Ice Cream because the label failed to declare eggs in the ingredient statement.
Zimmer, Inc. is recalling Drop Lok Knee Braces because raw material labeled as latex-free was found to contain latex. The recall affects 131 units distributed in the US and internationally.
Zimmer, Inc. is recalling 546 units of Hinged Knee Supports because raw material labeled as latex-free actually contained latex.
Kroger is recalling Private Selection Chocolate Hazelnut Mascarpone Ice Cream because the label failed to declare eggs in the ingredient statement.
Zimmer, Inc. is recalling 649 units of Neoprene Tennis Elbow Supports because raw material labeled as latex-free actually contained latex.
Zimmer, Inc. is recalling 2,222 units of Cartilage Knee Braces because raw material labeled as latex-free actually contained latex.
Fong Kee Tofu Co., Inc. is recalling Soy Bean Cake products because they contain wheat, a sub-ingredient of soy sauce, that is not declared on the label.
Flawless Beauty LLC is recalling Laroscorbine Platinium injectable solution because it was marketed without an approved NDA/ANDA and includes drug claims to act as an antidote.
First Aid Only is recalling Smart Tab First Aid ezRefill System Ibuprofen boxes that were accidentally filled with aspirin packs.
The Anspach Effort, Inc. is recalling 30 Anspach Cutting Burs (REF L-3SD) because the product code S-3SD was included, which is shorter than the labeled product.
Ortho Development Corporation is recalling five PS-C Femoral Nonporous Rt Sz 6 knee implant components because pegged versions were found in boxes labeled for the pegless version.
Konsyl Pharmaceuticals is recalling 6,286 bottles of Psyllium Fiber capsules because the label lists an inaccurate strength for the active ingredient.
Gold Medal Products is recalling 137 containers of Cajun Savory that were packed in Hot & Spicy containers. The recall covers distribution in nine US states and Bermuda.
Transatlantic Foods is recalling 449,000 pounds of pork products because labels falsely claimed the items contained no antibiotics.
Karl Bissinger LLC is recalling Bissinger's Dark Chocolate Bunny Ears because milk chocolate is packaged in dark chocolate packaging without milk listed on the ingredient statement.
Bread Stop Bakery is recalling 80 loaves of Flaxseed Bread because an anti-stick spray containing soy lecithin was used during manufacturing, but soy was not declared on the label.
Bread Stop Bakery is recalling 100 loaves of Amaranth bread because soy lecithin was used in manufacturing but not declared on the label.