State
73,833 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 73,833 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
Reser's Fine Foods is recalling Walmart Redskin Potato Salad due to potential Listeria monocytogenes contamination from a recalled onion lot.
Hospira is recalling PlumSet IV administration sets because intravenous fluid may leak at the secondary port. The recall covers 3,920,932 units distributed in the US and Canada.
Newmar is recalling 152 model year 2017 motorhomes because front fascia wood trim may separate and contact occupants, potentially causing loss of vehicle control.
Keenford Limited is recalling about 84,000 iMoto self-balancing scooters because their lithium-ion batteries can overheat, smoke, catch fire, or explode.
CareFusion 303, Inc. is recalling 69,693 Alaris System PC Units because the RESTORE feature may incorrectly populate patient weight for specific infusion modules.
Elekta is recalling 69 MOSAIQ Oncology Information System units because scrolling the mouse wheel could accidentally change the selected treatment plan.
Nephron Pharmaceuticals is recalling 11,208 cartons of Sodium Chloride Inhalation Solution because internal dye tests failed to confirm vial integrity.
Hospira is recalling Symbiq Two Channel Infusers due to frequent false occlusion alarms that may delay or interrupt patient therapy.
Hype Wireless is recalling about 25,000 Roam brand self-balancing scooters because their lithium-ion batteries can overheat, posing a risk of smoking, fire, or explosion.
Smith & Nephew is recalling Legion Hinge Knee femoral assemblies because the cement application surface is below specification.
Medical Depot Inc. is recalling 123,125 pairs of Universal Quick Adjust aluminum crutches because the metal tips may fail and detach from the ground.
PTX Performance Products is recalling about 4,900 Airwalk self-balancing scooters because the lithium-ion batteries can overheat, posing a risk of fire or explosion.
Medtronic is recalling 368 Sagittal Saw devices because testing identified a potential for fluid leakage into the motor during use.
Hospira is recalling approximately 3.9 million LifeShield IV administration sets because fluid may leak at the secondary port.
Yuka Clothing is recalling about 800 self-balancing scooters sold nationwide and online because the lithium-ion battery packs can overheat, posing a risk of smoking, fire, or explosion.
Nephron Pharmaceuticals is recalling 13,692 cartons of Sodium Chloride Inhalation Solution due to a failure in the internal dye ingress test, which raises concerns about the sterility of the vials.
Baxter Healthcare is recalling 10,054 units of PrismaSate BGK2/0 Dialysis Solution for Continuous Renal Replacement Therapy because of leaks near the top of the bags.
Embrace Technologies is recalling Little Lotus baby swaddles and sleeping bags because shoulder snaps can break or detach, posing a choking hazard to young children.
Siemens Healthcare Diagnostics Inc. is recalling 487 Hettich Centrifuge Modules due to premature bucket failures. The units were distributed nationwide.
Medical Depot Inc. is recalling 123,125 pairs of Universal Quick Adjust aluminum crutches because the metal tips may fail.
Medical Depot Inc. is recalling 123,125 pairs of Universal aluminum crutches because the bottom metal tips may fail.
Medical Depot Inc. is recalling 123,125 pairs of EZ adjust aluminum crutches because the tip may fail, posing a risk of injury.
Motor Coach Industries is recalling 2015-2016 J4500 buses because improperly installed window hardware may allow windows to open unexpectedly, increasing ejection risk.
Hospira is recalling specific LifeShield IV administration sets because intravenous fluid may leak at the CLAVE secondary port.
Hospira is recalling specific lots of Lifeshield IV administration sets because intravenous fluid may leak at the secondary port.