State
73,741 recalls have nationwide distribution and so reach Utah. 4,914 additional recalls listed Utah specifically in their distribution scope.
Of the 4,914 recalls naming Utah we have scored against our rubric, 524 (11%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 1,350 (27%) are Severe.
Which agencies issued them
These figures cover only the 4,914 recalls whose distribution notice names Utah specifically. The 73,741 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
Pacira Pharmaceuticals is recalling 910 vials of Exparel (Bupivacaine) because the drug was found to be sub-potent and out of specification.
Brasseler USA is recalling 387 units of 3.5 mm twist drills that were incorrectly laser etched as 2.5 mm.
Miami Device Solutions is recalling 15 units of Right Proximal Humerus Plates because they may be improperly identified as left.
Theralase Inc. is recalling 41 TLC-2000 Therapeutic Medical Laser Systems because they were shipped without required Unique Device Identification (UDI) labels.
Theralase Inc. is recalling 306 TLC-2002 Power Packs for the TLC-2000 Therapeutic Medical Laser System because they were shipped without a Unique Device Identification (UDI) label and incorrectly labeled as CE Marked.
Ruiz Food Products is recalling approximately 55,013 pounds of frozen breakfast burritos that may contain pieces of plastic. No injuries have been reported.
Bass Pro is recalling MR. STEAK four and five burner gas grills because the fuel line can melt and cause a fire.
Marion Body Works is recalling 2018-2019 Spartan Gladiator and Metro Star emergency response chassis because a brake relay valve defect may cause extended stopping distances.
Jayco is recalling 2019-2020 White Hawk travel trailers because the rear emergency escape window cannot fully open due to a ladder. Owners should contact dealers for a free repair.
Keystone RV Company is recalling 2020 Springdale trailers because the Federal Identification Tags list incorrect rim, tire, and pressure information.
ARBOC Specialty Vehicles is recalling 2017-2019 Spirit of Freedom and Spirit of Mobility vehicles because the roof hatch handle may break, preventing emergency egress.
Proterra is recalling 2019 Catalyst buses because a software update may have disabled brake interlock warnings, increasing the risk of fire or crash.
Surly Bikes is recalling about 5,139 front bicycle racks because they can loosen and contact the front wheel, posing crash and injury hazards.
Volkswagen is recalling 2013-2015 Jetta Hybrid vehicles because hairline cracks in the transmission can cause oil leaks and sudden loss of drive power, increasing crash risk.
Trek is recalling about 2,840 Super Commuter+ 8S electric bicycles because a front fender bolt can unthread, causing the wheel to detach and posing a fall hazard.
Daimler Trucks North America is recalling 145 school buses due to loose fan hub bolts that could damage components or detach, risking injury during an uncontrolled stop.
WilliamsRDM is recalling StoveTop FireStop Rangehood and Microhood automatic cooktop fire suppressors because they may fail to activate and suppress fires.
Mercedes-Benz is recalling one 2020 GLE 450 4MATIC because third-row headrests may not hold in place, increasing injury risk in a crash.
Mercedes-Benz is recalling 2019 AMG E53, E63, and E63S models because incorrect driver air bags and software may be installed, increasing injury risk in crashes.
Honda is recalling 2019-2020 CR-V vehicles because improperly manufactured rear subframe bolts may loosen, allowing the subframe to separate and increasing crash risk.
DaVinci is recalling about 3,000 Bailey bassinets because support legs can break, posing a fall hazard to infants. Consumers should stop using them and contact the company for a repair kit.
AuroMedics Pharma LLC is recalling Aurobindo Ranitidine Capsules 300 mg because N-nitrosodimethylamine (NDMA) was detected in the product.
New Vitalis Pharmacy is recalling Testosterone Cypionate and Propionate oil injection solutions due to a lack of sterility assurance.
AVKARE Inc. is recalling specific lots of Ranitidine Tablets 300 mg because the active ingredient contained the impurity N-nitrosodimethylamine (NDMA).
AVKARE Inc. is recalling specific lots of Ranitidine Tablets 150 mg because the active ingredient contained the impurity N-nitrosodimethylamine (NDMA).