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.
Becton Dickinson is recalling BD Stimex Insulated Needles because the instructions for use lack general contraindications.
Becton Dickinson is recalling BD Regional Block Needles because the instructions for use lack general contraindications, as advised by the European Notified Body.
Gem City Fine Foods is recalling 164 Vegan Chocolate Cakes because the nutrition facts panel and ingredient list were incorrect.
Neocis, Inc. is recalling 100 units of Gen 2 Anterior Chairside Splints due to potential mislabeling. The affected units were distributed to facilities in seven states.
The Yukon polyaxial screw component in the Yukon Spinal System was recalled because it was incorrectly laser marked with wrong dimensions.
Sun Pharmaceutical Industries Inc. is recalling Testosterone Cypionate Injection due to an incorrect lot number on secondary packaging.
GH Foods CA LLC is recalling Asian Noodle Salad Kits because the ingredient 'Eggs' was not listed on the retail scale label, despite a 'may contain' warning.
GH Foods CA LLC is recalling Spinach and Basil Pasta Salad Kits because the ingredient 'Eggs' was not listed on the retail scale label, despite a 'may contain' warning.
GH Foods CA LLC is recalling Italian Pasta Salad Kits sold at Whole Foods and Amazon because the label failed to list eggs as an ingredient, despite a 'may contain' warning.
Fujifilm is recalling Synapse PACS Software versions 5.1 and higher because it may display incorrect patient information or PET/CT values.
GH Foods CA LLC is recalling Smoked Mozzarella Pasta Salad Kits sold at Whole Foods because the ingredient 'Eggs' was not listed on the retail scale label.
GH Foods CA LLC is recalling Pesto Pasta Salad Kits because the ingredient 'Eggs' was not listed on the retail scale label, despite a 'may contain' warning.
Allergan is recalling Refresh Relieva Preservative-Free eye drops because the packaging is missing the instructions for use insert.
Skeletal Kinetics is recalling 49 units of OsteoVation bone filler kits because the mixing instructions on the card do not match the Instructions for Use.
Beckman Coulter is recalling 276 units of ACCESS SARS-CoV-2 IgG Quality Control cards due to a label error regarding standard deviation values.
Exactech is recalling 14 Equinoxe Humeral Stem devices because packages may include incorrect Instructions For Use (IFU).
Smiths Medical ASD Inc. is recalling 4,440 Portex Acapella DH Vibratory PEP Devices because shipping boxes may contain the wrong model number.
Skeletal Kinetics is recalling 2 units of OsteoVation Inject Bone Filler Kits because of a discrepancy between the Mixing Instruction Card and the Instructions for Use.
Nissan is recalling 2020 INFINITI QX50 vehicles because the tire and loading information placard may be illegible, potentially leading to incorrect tire installation or overloading.
Fresenius Medical Care is recalling 198 drums of Citrasate Liquid Acid concentrate because sodium and/or calcium levels were below manufacturing specifications.
Fresenius Medical Care is recalling 123 bottles of Naturalyte Liquid Acid concentrate due to conductivity deviations and low calcium levels.
The FDA is recalling Divvies Vegan and Nut Free Vanilla Cupcakes because they contain undeclared milk and egg ingredients.
Fresenius Medical Care is recalling NaturaLyte Liquid Acid concentrate bottles because sodium and/or calcium levels were below manufacturing specifications.
Ansh Labs is recalling 327 SARS-CoV-2 IgM ELISA kits to update instructions and reduce the risk of false test results.
Fresenius Medical Care is recalling 27 drums of NaturaLyte Liquid Acid concentrate because sodium and/or calcium levels were below manufacturing specifications.