Hazard
9,610 recalls in our database tag this hazard, drawn from FDA, USDA FSIS, CPSC, and NHTSA source notices.
Of the 9,610 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 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.
Cardinal Health is recalling Gomco Style Circumcision Clamp Trays because two lots were labeled as containing 1.1cm clamps but actually contained 1.3cm clamps.
Yummy Earth Inc. is recalling YumEarth Organics Gummy Worms because the outer and individual packages list different carbohydrate amounts.
Yummy Earth Inc. is recalling YumEarth Organics Gummy Bears due to inconsistent carbohydrate labeling on the packaging.
Immuno-Dynamics, Inc. is recalling PerCoBa and Synertek colostrum lozenges because the labels state 'contains dairy' instead of 'contains milk.'
Richard-Allan Scientific is recalling Type 3 Paraffin because customers found Type 6 Paraffin inside the boxes. The product is used for histology tissue processing.
Jubilant DraxImage is recalling Sodium Iodide I 131 Diagnostic capsules due to a label error regarding the declared strength.
Immuno-Dynamics, Inc. is recalling PerCoBa and Synertek colostrum powder because the labels state 'contains dairy' instead of 'contains milk.'
Apace KY LLC is recalling 291 cartons of Minocycline Hydrochloride Capsules because individual blisters are mislabeled with an incorrect lot number.
ProSupps is recalling Dr. Jekyll Intense Pump Pre Workout due to potential mislabeling and the presence of the non-dietary ingredient Picamilon.
ProSupps USA LLC is recalling Mr. Hyde Intense Energy Pre-Workout supplements because they may contain the undeclared non-dietary ingredient Picamilon.
Nestle USA is recalling Maggi Chicken Flavor Bouillon tablets because they contain undeclared wheat, posing a risk to individuals with wheat allergies or celiac disease.
Fresh Creative Foods is recalling H-E-B Tartar Sauce because it contains undeclared fish due to a labeling error.
Hale Products Inc. is recalling portable pumps with Yanmar diesel engines due to a mislabeled dashboard warning light that could hinder fire suppression.
ProSupps USA LLC is recalling Dr. Jekyll Intense Pump Pre Workout because it may contain the non-dietary ingredient Picamilon.
Biomet Spine is recalling specific Solitaire Ti Spacers because they are mislabeled as having a 12-degree lordotic angle when the actual angle is 6 degrees.
Safecor Health is recalling 23 cups of Donnatal Elixir because the label incorrectly lists the dose as 5 ml instead of 10 ml.
ProSupps USA LLC is recalling 33 units of Mr. Hyde Intense Energy Pre-Workout because the product may contain undeclared Picamilon.
Medtronic is voluntarily removing a single Ascenda Intrathecal Catheter kit due to incorrect outer package labels that may result in missing components.
ProSupps USA LLC is recalling Mr. Hyde Intense Energy Pre-Workout supplements because they may contain the undeclared non-dietary ingredient Picamilon.
Siemens is recalling 726 Symbia gamma camera systems worldwide to provide supplemental instructions clarifying the proper collimator change procedure.
Pfizer is recalling 63,636 bottles of Robitussin Peak Cold Liquid nationwide due to a label mix-up. Consumers should stop using the product and return it to the point of purchase.
Genzyme Corporation is recalling 24 vials of Lumizyme (alglucosidase alpha) because the packaging may have incorrect or missing lot and expiration dates.
King Soopers is recalling Apple Strudel 5 Count packages because the ingredient label fails to declare pecans.
Northwest Specialty, Inc. is recalling dried lactose powder sold as Wine-King Beer-King because the label fails to declare whey or milk.
Cook Medical is voluntarily recalling specific lots of Ascend AQ Ureteral Dilation Balloon Catheter Sets and Ultraxx Nephrostomy Balloon Sets due to a labeling error where packages may contain the wrong product.