State
73,817 recalls have nationwide distribution and so reach Utah. 4,916 additional recalls listed Utah specifically in their distribution scope.
Of the 4,916 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 1,351 (27%) are Severe.
Which agencies issued them
These figures cover only the 4,916 recalls whose distribution notice names Utah specifically. The 73,817 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
Elekta is recalling the MOSAIQ Medical Charged-Particle Radiation Therapy System because a software error inverts vertical table shifts, potentially directing therapy to incorrect areas.
ImprimisRx is recalling compounded Timolol ophthalmic drops because they were made with non-pharmaceutical grade PEG 40 Castor Oil due to supplier mislabeling.
Beckman Coulter is recalling LH 750, LH 780, and LH 500 analyzers because they may fail to flag blasts in some blood samples.
Cardinal Health is recalling Presource surgical kits because they contained BD SafetyGlide needles with loose polypropylene particulate in the fluid path.
Heartland is recalling 2018 Sundance XLT TT recreational trailers because rear axles were installed backwards, which may reduce braking ability or cause brakes to lock up.
MicroVention is recalling 34 units of Traxcess 7 Mini Guidewires because the hydrophilic coating may delaminate from the device.
Beckman Coulter is recalling HmX CP and HmX AL analyzers because they may fail to flag or detect blasts in rare blood sample situations.
Merge Healthcare is recalling Merge Unity software versions 10.0 through 11.1.2 Patch 4 because the software fails to identify atypical hyperplasia, leading to incorrect Gail Risk calculations.
Qualigen Inc is recalling specific lots of its Vitamin D Complete Immunoassay Kit because they may produce falsely low results.
ImprimisRx is recalling 19 bottles of compounded Latanoprost ophthalmic drops because they contain non-pharmaceutical grade PEG 40 Castor Oil due to supplier mislabeling.
ImprimisRx is recalling 16 bottles of compounded Timolol-Latanoprost ophthalmic drops because non-pharmaceutical grade PEG 40 Castor Oil was used due to supplier mislabeling.
Lupin Pharmaceuticals is recalling 12,888 bottles of Famotidine for Oral Suspension due to CGMP deviations. The FDA classified this voluntary recall as Class III.
Chrysler is recalling 2013-2017 RAM trucks with specific Cummins diesel engines because a water pump defect may leak coolant and increase the risk of an engine compartment fire.
Highland Ridge RV is recalling 2018 Open Range 3X fifth wheel trailers because tire size labels may be incorrect, potentially leading to the installation of wrong-sized tires.
Altec is recalling 2011-2017 LS63 Aerial Devices because the jib mast may bend under load, increasing the risk of injury to nearby individuals.
Trek Tire is recalling specific Dunlop GrandTrek PT3A tires manufactured in December 2016 because they lack complete DOT identification markings, which may increase crash risk.
Micro Bird is recalling 25 units of 2016 G5 school buses because seat mounting studs may lack adequate padding, increasing injury risk in rear-end collisions.
Gillig is recalling 2013-2016 Low Floor buses because a steering component may fail, causing loss of power assist and increased crash risk.
Nantucket Distributing is recalling Bimini patio set chairs because the fabric seat can tear, posing a fall hazard. Consumers should stop using the chairs and return them for a refund.
Eldorado is recalling 2015 Axess transit buses because front suspension link rod clamps may not be properly torqued, which can loosen the link rod and decrease steering ability.
Thor Motor Coach is recalling 2014-2016 motorhomes because windshield wipers may fail due to incorrect installation, increasing crash risk.
KZRV is recalling 2017-2018 Connect, Spree, and Sport Trek trailers because a missing fuse in the awning light circuit may cause wire overheating and fire.
L.L. Bean is recalling toddler sweater fleece pullovers because the snaps can detach, posing a choking hazard to young children.
Smith is recalling Quantum ski and snowboard helmets because the buckle can disengage, posing a risk of head injury. No injuries have been reported.
J-Tech is recalling specific Icon Alliance motorcycle helmets because faulty stitching may allow the chin strap to separate, increasing injury risk in a crash.