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.
Arrow International Inc. is recalling 789 units of Arrow Pressure Injectable PICC catheters because they contain a 40cm catheter instead of the required 50cm catheter.
Merit Medical Systems is recalling 173 units of Laureate Hydrophilic Guide Wire due to a labeling discrepancy where the product was mixed with a different lot.
Pega Medical Inc. is recalling 48 units of the Fassier-Duval IM Telescopic System because the outer package label listed the incorrect device length.
Ev3 is recalling two lots of EverCross PTA Dilatation Catheters because of a discrepancy in the balloon and delivery catheter lengths printed on the product labeling.
Branan Medical is recalling ToxCup Drug Screen Cups because the lid labels may contain incorrect result interpretation graphics.
Arrow International is recalling 170 units of Arrowgard Blue Plus Antimicrobial Multi-lumen Central Venous Catheters because the lidstock incorrectly lists the catheter length as 16CM instead of 20CM.
Abbott Molecular is recalling 20 kits of CEP 8 SG ASR Probe that contained the wrong probe. The kits contained Vysis CEP 4 probe instead of the expected CEP 8 probe.
Merit Medical Systems is voluntarily recalling specific lots of Laureate Hydrophilic Guide Wires due to a discrepancy between carton and unit labeling.
Upsher Smith Laboratories is recalling 36 bottles of Oxandrolone Tablets, USP, 10 mg, because they were packaged without primary labels.
Knockum Hill Bar-B-Que is recalling approximately 350 pounds of hickory smoked barbecue pork products because they contain an undeclared soy allergen.
Haute Health is recalling Virilis Pro dietary supplements because they may contain unapproved active ingredients found in FDA-approved erectile dysfunction drugs.
Forest River is recalling 152 model year 2014 XLR XLT29HSF travel trailers because the Federal Certification label lists incorrect weight ratings, which could lead to tire failure.
Tedesco LLC is recalling 120/5.1 oz cups of Graeter's Cookies and Cream ice cream because the label fails to list wheat and soy allergens.
Whole Foods Market is recalling Chipotle Chicken Wraps because they contain undeclared anchovies, a fish allergen, in the filling.
John B. Sanfilippo & Son Inc. is recalling Fisher Honey Roasted Peanuts because the product contains wheat, an allergen not declared on the label.
Terumo is recalling 37 units of Cardiovascular Procedure Kits in California due to an incorrect customer notification label applied to the Tyvek lid.
Ortho-Clinical Diagnostics is recalling VITROS CRBM Slides, Lot 3920-0080-8403, because they may produce biased carbamazepine results.
Magno Humphries Laboratories is recalling Vitamin E softgels because the main label states 1000 IU while the Supplement Facts panel indicates 200 IU.
Codman & Shurtleff is recalling 9,445 units of Certas Programmable Valves to ensure customers have tools to verify valve settings and location on x-ray images.
Synthes is recalling CMF Battery Powered Drivers because the packaging graphics suggest off-label use with taps, which is not intended.
Solta Medical is recalling 1,077 Fraxel DUAL 1550/1927 Laser Systems because obsolete treatment cards may contain incorrect indications for treating Melasma.
Synthes, Inc. is recalling 20 Hohmann retractors because they were mis-etched with the wrong part number.
Kraft Foods Group is recalling approximately 96,000 pounds of Oscar Mayer Classic Wieners because the packages may contain cheese dogs with undeclared milk.
Bolzano Artisan Meats is recalling approximately 5,723 pounds of salami products because they were misbranded with the USDA Mark of Inspection without federal authorization.
Breg Inc is recalling two knee support models because they contain latex but lack the required caution label.