State
73,584 recalls have nationwide distribution and so reach Wyoming. 3,226 additional recalls listed Wyoming specifically in their distribution scope.
Of the 3,226 recalls naming Wyoming we have scored against our rubric, 762 (24%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 681 (21%) are Severe.
Which agencies issued them
These figures cover only the 3,226 recalls whose distribution notice names Wyoming specifically. The 73,584 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
Kia Motors America is recalling 2020-2021 Stinger vehicles with a fuel gauge software error that may cause inaccurate readings, risking unexpected fuel depletion and vehicle stalling.
Yamaha is recalling 2016-2021 FJR1300 motorcycles because a previous software update may prevent the engine from accelerating as intended, increasing crash risk.
Tiffin Motorhomes is recalling certain 2018–2022 recreational vehicles with sofa seat belts that may not be correctly installed. Unsecured passengers face increased injury risk in a crash.
Cottrell is recalling 2019-2022 2-Car Carriers because four side-rear reflex reflectors are missing, which reduces visibility and increases crash risk.
Mercedes-Benz is recalling certain 2021 GLB250 and AMG GLB35 vehicles because the driver-side window airbag may not be properly mounted to the A-pillar, which could prevent proper deployment during a crash.
Volvo Trucks North America is recalling 2021 VNL vehicles because a machining defect in the power steering pump may cause a loss of steering assist, increasing crash risk.
Kubota is recalling about 48,875 RTV-X1100C utility vehicles from model years 2013 through 2021 because floor mats can warp or degrade and interfere with the throttle pedal, creating crash and injury risks.
Tracker Marine is recalling 2022 Ranger Trail boat trailers because improperly spaced fenders may contact tires, causing premature wear and potential tire failure.
Supreme is recalling 2019-2020 Dry Freight Body vehicles because a rearward-aiming license plate light may increase crash risk.
Backyard Play Systems is recalling four outdoor playset models due to an entrapment hazard in the wooden roof design. Children can become trapped in gaps between the roof structure and gable decoration.
ROSA One 3.1 surgical guidance system recalled due to a software anomaly causing inaccurate electrode placement during brain and spine surgery. Manufacturer received 3 complaints related to the issue.
Mack Trucks is recalling 2021 Granite and LR vehicles because a power steering pump defect may cause loss of assist, increasing crash risk.
Daimler Vans USA is recalling one 2020 Mercedes-Benz Sprinter because incorrect-size front brake discs may extend stopping distance and increase crash risk.
Siemens is recalling Advia Chemistry Urinary/Cerebrospinal Fluid Protein reagent due to potential reagent carryover that may cause falsely depressed Hemoglobin A1c results, which could affect clinical decisions about patient treatment.
Volkswagen is recalling 2022 Tiguan vehicles with a loose brake pipe nut near the right-front wheel well. The loose nut could cause brake fluid to leak, reducing braking power and increasing crash risk.
Siemens Healthcare is recalling Atellica CH Urinary/Cerebrospinal Fluid Protein reagent due to potential carryover causing falsely depressed Hemoglobin A1c results that may affect clinical decision-making.
Volkswagen is recalling one 2021 ID.4 vehicle with a defective steering gear. A missing or incorrectly assembled drive bushing may cause loss of steering control and increase crash risk.
Olympus recalls ASC PneumoLiner surgical devices due to incorrect orientation of the containment bag that deploys upside down. This increases the risk of trapping bowel tissue during gynecologic laparoscopic surgery.
Rolls-Royce is recalling 2019-2022 Phantom vehicles because the central display may not raise correctly, partially blocking the rearview camera image.
Xstrahl's Concerto software used in X-ray therapy systems may fail to update treatment parameters for a second beam when a treatment plan is edited. This could result in error messages and incorrect treatment delivery.
Potomac River Group recalls 62 RAPTAR Laser Range Finders (Model G02) nationwide. The devices can be field-modified to enable higher-power visible and infrared lasers, posing eye injury risk from uncontrolled laser radiation.
Usines Giant Factories is recalling about 168 gas water heaters with Emerson control valves that can short circuit, overheat, and release carbon monoxide. The company will replace the control valve free of charge.
Smiths Medical is recalling 7136 Bivona Aire-Cuf Endotracheal Tubes due to inadequate pouch seals that compromise the sterile barrier. The issue affects specific lot numbers with 325mm shaft length.
Smiths Medical ASD Inc. is recalling 2,191 Bivona Uncuffed Wire Endotracheal Tubes due to inadequate pouch seals that compromise the sterile barrier. Affected devices have 325mm shaft lengths and were distributed nationwide and internationally.
AB SCIEX's Cliquid MD version 3.4 software may incorrectly calculate Internal Standard concentrations when users hide or leave the IS column empty in customized LC-MS/MS tests, potentially leading to incorrect analytical conclusions.