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.
Siemens is recalling Syngo.via software because it fails to save corrected report values, potentially sending outdated information to physicians.
Phadia Ab is recalling Phadia Prime software versions up to 2.1.4 to prevent the use of the 'OK to All' function when rejecting and retesting EliA assay samples.
Arrow International is recalling 930 Radial Artery Catheterization Kits because the included povidone iodine prep pads are labeled with an incorrect 36-month shelf life instead of 24 months.
Arrow International is recalling Arterial Access Trays because the included povidone iodine prep pads do not meet the 36-month shelf life requirement and must be labeled with a 24-month shelf life.
Aesculap Implant Systems LLC is recalling 270 DS Titanium Ligation Clip Appliers to update instructions for use, adding contraindications for living donor nephrectomies.
Arrow International is recalling Radial Artery Catheterization Kits because the included povidone iodine prep pads do not meet the 36-month shelf life requirement and should be labeled with a 24-month shelf life.
Arrow International is recalling 570 Radial Artery Catheterization Kits because the included povidone iodine prep pads are labeled with an incorrect 36-month shelf life.
Zimmer Biomet is recalling 22 A.L.P.S. MIS Calcaneus Locking Plate LG RT F.A.S.T. Guide inserts due to incorrect color anodization.
Pepsi Beverage Co is recalling 1,972 cases of Diet Pepsi because the cans are labeled to contain Sucralose but actually contain Aspartame.
Aesculap Implant Systems LLC is recalling DS Titanium Ligation Clips to update instructions for use, adding a contraindication for living donor nephrectomies.
Josie's Homestyle Pralines are being recalled because the label incorrectly lists cream instead of evaporated milk and omits butter sub-ingredients.
Arrow International is recalling Radial Artery Catheterization Kits because the included povidone iodine prep pads do not meet the 36-month shelf life requirement and should be labeled with a 24-month shelf life.
Arrow International is recalling Radial Artery Catheterization Kits because the included povidone iodine prep pads do not meet the 36-month shelf life requirement.
Gulf Stream is recalling 2017-2018 Conquest motorhomes because federal placards may list an incorrect Gross Vehicle Weight Rating, potentially leading to vehicle overload.
Wegmans is recalling Thai Sweet Chili Sauce cups because they contain undeclared egg, a major food allergen.
Wegmans is recalling Assorted Gyoza packaged with Thai Sweet Chili Sauce because the sauce contains undeclared egg.
Apollo Care is recalling 144 bags of Vancomycin IV solution because stability data does not support the assigned 90-day beyond use date.
Lancaster Fine Foods Inc. is recalling 1.5 oz. cups of Thai Sweet Chili Sauce because some cups were mislabeled as Spicy Mayonnaise Sauce.
IDLife, LLC is recalling IDLife Protein Bar Chocolate and Peanut Butter because the product contains almonds but does not declare them on the label.
Zimmer Biomet is recalling 24 hip implant packages labeled as size 7.5 Extended Offset Reduced Neck length that actually contained Size 4 Standard Reduced Neck length implants.
Vietti Acquisitions is recalling Southgate Hot Dog Chili Sauce because it contains egg and wheat that are not listed on the label.
Weis Markets is recalling store-made coleslaw sold in New York because the label failed to declare egg, a major food allergen, contained in the mayonnaise.
IDLife, LLC is recalling IDLife Kids Bar Chocolate and Mixed Berry because allergen testing detected almonds and coconut in a product labeled as nut-free.
Pinks Bakery Seattle, Inc. is recalling Marsee Baking brand Hippie Cookies because coconut is listed in the ingredients but not declared in the 'Contains' statement. The product was distributed in Oregon and Washington.
IDLife, LLC is recalling IDLife Snack Bar Chocolate and Almond because the product contains almonds but does not declare the presence of peanuts.