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.
Honda is recalling 2017 Clarity Fuel Cell vehicles because a software defect may cause reduced or complete power loss, increasing crash risk.
Elkay is recalling water coolers and bottle filling stations because internal screws can break, causing a loose grounding wire and shock hazard.
VTech is recalling Lights & Lullabies travel mobiles because the clamp can break, causing the mobile to fall and potentially injure an infant.
Forest River is recalling 2018 Palomino PaloMini recreational trailers because the propane bottle mounting bracket may break, allowing the bottle to detach and increasing the risk of injury or crash.
VTech is recalling Shake & Sing Elephant Rattles because the ears can break off, posing a choking hazard to young children.
Fieldbrook Foods is recalling ice cream variety packs due to potential Listeria monocytogenes contamination. The products were distributed nationwide, including Puerto Rico.
H.I.G. Corporation is recalling 522 cases of frozen tuna fillet saku because customer testing detected Listeria monocytogenes.
Fieldbrook Foods is recalling chocolate covered vanilla ice cream bars due to potential Listeria monocytogenes contamination. The products were distributed nationwide, including Puerto Rico.
Fieldbrook Foods is recalling Sundae Shoppe Raspberry Cream Ice Cream Bars due to potential Listeria monocytogenes contamination. The product was distributed nationwide, including Puerto Rico.
Fieldbrook Foods is recalling Orange Cream Ice Cream Bars sold under multiple brand labels due to potential Listeria monocytogenes contamination.
RaySearch Laboratories is recalling RayStation 6 software due to a defect in the proton QA module that may result in incorrect patient dosage calculations.
Merge Healthcare is recalling 1,150 power strips sold with the Merge Hemo System because an input resistor can overheat and cause the unit to smoke.
Pharmedium Services is voluntarily recalling 2,390 syringes of Phenylephrine HCL 100 mcg/mL due to a superpotent drug classification.
Zoll Manufacturing Corp. is recalling 33,670 LifeVest Wearable Defibrillators due to an incorrect service code that may prevent the device from detecting critical defects, potentially leading to defibrillation shock failure.
Boston Scientific is recalling ACCOLADE MRI SR Pacemakers due to reports of intermittent over-sensing of the Minute Ventilation sensor signal.
Roche Diagnostics is recalling 2,517 automated laboratory analyzers due to a software limitation that may cause sample mismatches.
Fuel Helmets is recalling specific models because the securing strap may fail in extreme temperatures, increasing injury risk in a crash.
Boston Scientific is recalling PROPONENT SR Pacemakers because reports indicate the Minute Ventilation sensor may intermittently over-sense signals.
Boston Scientific is recalling certain pacemakers due to reports of intermittent over-sensing of the Minute Ventilation sensor signal.
Boston Scientific is recalling ESSENTIO EL DR pacemakers due to reports of intermittent over-sensing of the Minute Ventilation sensor signal.
Boston Scientific is recalling ACCOLADE MRI EL DR pacemakers due to reports of intermittent over-sensing of the Minute Ventilation sensor signal.
Ventura Foods is recalling single-serve Italian dressing packets because a plastic foreign object was inadvertently introduced into the product stream.
Ventura Foods is recalling 18 cases of House Recipe Bleu Cheese Dressing & Dip because a plastic foreign object was inadvertently introduced into the product stream.
Boston Scientific is recalling ESSENTIO DR Pacemakers because the Minute Ventilation sensor may intermittently over-sense signals.
Boston Scientific is recalling VISIONIST CRT-P pacemakers because the Minute Ventilation sensor may intermittently over-sense signals.