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.
Medicamat is recalling 71 units of the Punch Hair Matic surgical hair transplant device due to misbranded marketing literature.
WalkMed Infusion is recalling 797 Triton FP Infusion Pumps because the label on the right side contains an incorrect instruction.
Heraeus Kulzer is recalling BencoDental tartar and stain remover due to incorrect labeling on the immediate container.
Synthes, Inc. is recalling 45 units of 5.0mm Variable Locking Screws because one package contained the wrong insert.
Medtronic is recalling O-arm Imaging Systems because a review found gaps in compliance with FDA labeling requirements for user information.
McKesson Technologies is recalling 10 units of the Anesthesia Care system because patient case data did not match the patient data, including data from another case.
Mako Surgical Corporation is recalling 41 units of the Restoris Multicompartmental Knee System because the product may be mislabeled, which could result in the incorrect implant being used.
DJO Surgical is recalling 10 units of FMP X-alt Acetabular Liners that were mistakenly packaged and labeled as different models and sizes.
Horiba Medical is recalling ABX PENTRA calibrators and controls because target values for the Creatinine Rate Blank Method were updated.
AMO Puerto Rico Manufacturing is recalling 169 units of TECNIS CL Foldable Silicone IOLs because they may be labeled with the incorrect diopter power.
Medefil Incorporated is recalling Heparin I.V. Flush Syringes because the barcodes on the master cartons do not match the printed product codes.
George's Inc. is recalling 29,200 pounds of seasoned raw chicken breast strips because the labels failed to declare soy protein and MSG.
Unified Grocers is recalling 12 oz. Ginger Snap Cookies because they contain undeclared egg. The recall affects products distributed in California, Arizona, and Nevada.
UNFI is recalling Kinnikinnick Kinni-Kwik Bread & Bun Mix nationwide due to undeclared milk. Consumers with milk allergies should not consume the product.
Creation Gardens is recalling Creation Special Snack Mix because the packaging lacks required ingredient and allergen statements, including peanuts, tree nuts, soy, and wheat.
Newman's Own is recalling Salsa Con Queso, Medium All Natural, 16 oz. jars nationwide due to undeclared wheat.
E. Franco & Co. is recalling Brazo gitano rolled cakes with guava paste filling sold in Puerto Rico because they contain undeclared wheat.
E. Franco & Co. is recalling Brazo gitano rolls with papaya-cheese filling sold in Puerto Rico due to undeclared wheat.
E. Franco & Co. Inc is recalling approximately 2,300 rolls of Brazo gitano (rolled cake) with pineapple paste filling because the product contains undeclared wheat. The recall is limited to Puerto Rico.
L.M. Noodle Company is recalling Marlyce's Homemade Style Noodles because the label fails to declare wheat flour, a major allergen.
The Popcorn Factory is recalling heart-shaped popcorn balls because the Nutrition Facts and allergen labels were not applied to the individual pieces. The product contains milk and soy allergens.
Philips is recalling 7,157 HeartStart XL+ Defibrillators because the battery charge time at high temperatures is slightly longer than the 3 hours stated in the labeling.
Smith & Nephew is recalling Renasys EZ canisters to modify the bacterial overflow guard and update product labeling.
NxStage Medical is recalling 969 cases of PureFlow-B Solution due to mislabeling. The product is used in hemodialysis systems.
Green Mountain Coffee Roasters is recalling 8,928 boxes of Newman's Own Organic Coffee K-Cups because some caffeinated packs were incorrectly labeled as decaffeinated.