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.
PharMEDium Services is recalling 79 Ropivacaine HCl IV pumps because of incorrect or missing lot and expiration dates.
PharMEDium Services is recalling 147 Ropivacaine HCl IV pumps nationwide because of incorrect or missing lot and expiration dates.
PharMEDium Services is recalling 22 Ropivacaine HCl pumps nationwide because of incorrect or missing lot and expiration dates.
PharMEDium Services, LLC is recalling 21 pumps of Ropivacaine HCl 0.2% injection due to incorrect or missing lot and expiration dates.
The Kroger Co is recalling Dessert Cups yellow sponge cakes because the packaging fails to list milk in the allergen statement, despite it being an ingredient.
Kroger is recalling Bakehouse Bread Artisan Cranberry Orange Bread because the label fails to list pecans or tree nuts in the allergy statement.
Onkos Surgical, Inc. is recalling four units of the Eleos Limb Salvage System Segmental Stem due to incorrect collar size labeling.
ProSupps USA LLC is recalling specific Mr. Hyde Fruit Punch products because they are potentially mislabeled and contain the non-dietary ingredient Picamilon.
ProSupps USA LLC is recalling 6,348 units of Dr. Jekyll V2 Watermelon domestic because the product is potentially mislabeled and contains the non-dietary ingredient Picamilon.
ProSupps USA LLC is recalling 28,045 units of Mr. Hyde Green Apple supplements because they contain the non-dietary ingredient Picamilon.
Onkos Surgical is recalling four units of the Eleos Limb Salvage System Segmental Stem due to incorrect collar size labeling.
Onkos Surgical is recalling four units of the ELEOS Limb Salvage System Segmental Stem because the device collar size was incorrectly labeled as 25 mm instead of 32 mm.
ProSupps USA LLC is recalling Mr. Hyde Watermelon supplements because they contain the non-dietary ingredient Picamilon.
ProSupps USA LLC is recalling 3,045 units of Dr. Jekyll V2 Green Apple International because the product is potentially mislabeled and contains the non-dietary ingredient Picamilon.
Exactech is recalling 477 Novation Calcar Planer Guide Tips to update labeling with a caution about instrument breakage.
ProSupps USA LLC is recalling 34,124 units of Mr. Hyde Blue Razz (V2) because the product contains the non-dietary ingredient Picamilon.
American Pharmaceutical Ingredients LLC is recalling Doxycycline Hyclate USP active pharmaceutical ingredient due to misbranding. The product is subject to FDA Import Alert 66-66.
ProSupps USA LLC is recalling 698 units of Dr. Jekyll V2 Orange Burst because the product is potentially mislabeled and contains the non-dietary ingredient Picamilon.
ProSupps USA LLC is recalling Dr. Jekyll 30 Fruit Punch because it is potentially mislabeled and contains the non-dietary ingredient Picamilon.
CryoLife, Inc. is recalling 705 boxes of BioGlue Surgical Adhesive because 9 boxes had incorrect lot numbers on their courtesy labels.
Medtest Holdings is recalling Pointe Scientific Liquid Creatine Kinase Reagent Sets because the product insert does not match the approved premarket notification.
Medtest Holdings is recalling Pointe Scientific CRP calibrator and standard sets because vial labels incorrectly list units as mg/dl instead of mg/L.
Euro Diagnostica AB is recalling 501 units of DIASTAT ANA kits because the packaging displayed the original expiration date instead of the shortened one.
L. Perrigo is recalling 1,998 Walgreens Daytime and Nighttime Cold & Flu combo packs in Illinois because the packaging sleeve incorrectly identifies the contents as Day-Night Cold and Flu instead of Day-Night Cough Liquid.
Medtest Holdings is recalling five CK-MB Isoenzyme Control Kits because the product labeling contains an incorrect control range.