State
73,809 recalls have nationwide distribution and so reach Oklahoma. 5,823 additional recalls listed Oklahoma specifically in their distribution scope.
Of the 5,823 recalls naming Oklahoma we have scored against our rubric, 1,040 (18%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 1,494 (26%) are Severe.
Which agencies issued them
These figures cover only the 5,823 recalls whose distribution notice names Oklahoma specifically. The 73,809 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
Jayco is recalling 2017-2018 Eagle 333BHOK travel trailers because the safety chains are rated below the vehicle's weight limit, posing a crash risk if the trailer detaches.
Harley-Davidson is recalling 2008-2011 ABS-equipped motorcycles because brake fluid deposits may cause the ABS valve to stick, reducing braking ability and increasing crash risk.
Jayco is recalling 2018 Eagle travel trailers because the furnace can cause the cooktop flame to go out while gas continues to flow, creating an explosion risk.
Jayco is recalling 2018 Eagle travel trailers because the Gross Vehicle Weight Rating label may be incorrect, potentially allowing the vehicle to be overloaded.
Vogue Tyre & Rubber is recalling specific Signature V tires because they lack date codes on the sidewall, which may prevent owners from identifying recalled tires.
Highland Ridge RV is recalling 84 units of the 2018 Open Range light travel trailer because the Federal Label lists an incorrect Gross Axle Weight Rating.
Mitsubishi is recalling specific 2008-2012 models because a cracked drive belt tensioner flange may cause the belt to detach, leading to engine stalling and increased crash risk.
Mitsubishi is recalling specific 2007-2010 models because the sunroof glass may detach and become a road hazard, increasing crash risk.
Mitsubishi is recalling 2013-2016 Outlander and Outlander Sport vehicles because water may cause parking brake parts to corrode and bind, potentially preventing the brake from engaging.
Rockler is recalling I-Semble Murphy Bed hardware kits because they may not provide sufficient bracing, posing tip-over and entrapment hazards.
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.
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.