State
73,100 recalls have nationwide distribution and so reach Nevada. 5,696 additional recalls listed Nevada specifically in their distribution scope.
Of the 5,696 recalls naming Nevada we have scored against our rubric, 951 (17%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 1,479 (26%) are Severe.
Which agencies issued them
These figures cover only the 5,696 recalls whose distribution notice names Nevada specifically. The 73,100 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
Daimler Trucks is recalling certain Freightliner and Western Star trucks because brake lights may fail to illuminate during automatic emergency braking, increasing crash risk. Dealers will update software at no cost.
McLaren is recalling 2020-2023 GT vehicles because the hood latch cable may have excessive tension, causing the hood to open unexpectedly and obstruct the driver's view.
Alliance RV is recalling certain 2024-2025 Valor travel trailers where the front bathroom outlet may lack Ground Fault Interrupter (GFI) protection. This missing safety feature can result in electrical shock.
Multiquip is recalling 2024 WTE5C and WTE5HP trailers because incorrect wiring may cause brakes to engage unexpectedly or fail to engage when turn signals are used.
Mercedes-Benz is recalling 2024 GLC 300 and AMG GLC 43 vehicles because improper welds on the engine carrier may cause loss of vehicle control.
Mercedes-Benz recalls 2019-2023 G 550 and 2019-2022 G63 AMG vehicles with faulty rear door latches that may fail to engage or prevent door operation, creating crash and injury risks.
Nova Bus is recalling 208 certain 2019-2024 LFS buses due to an auxiliary heater module that can cause electrical shorts and heating/defrosting failures, increasing fire risk and reducing windshield visibility.
Holley is recalling 736 Sniper 2 EFI Throttle Bodies that may be missing a fuel plug, creating a risk of fuel leaks and fire.
Airstream is recalling 2024 Trade Wind travel trailers because the air conditioner soft start device may overheat, increasing the risk of a fire.
Phoenix Motorcars is recalling certain 2019-2021 800V Catalyst and 2020-2022 ZX5 transit buses. The vehicle software may cause the radiator fan electrical circuit to overheat, increasing fire risk.
Chrysler is recalling certain 2019, 2021-2024 RAM 1500 vehicles because a software malfunction in the ABS control module may disable the electronic stability control system, increasing crash risk.
Chrysler is recalling MOPAR anti-lock braking system control modules used as replacement parts in certain Ram 1500 vehicles. A software malfunction may disable the electronic stability control system, increasing crash risk.
Delta Cycle Corp is recalling ceiling hoists with straps because plastic buckles can break when holding kayaks, canoes, or other large objects. The company has received four incident reports, including one minor injury.
Porsche is recalling 954 model year 2024 Taycan vehicles due to incorrect headlight control module software that may prevent parking lights from functioning when turn signals are activated, potentially reducing visibility and increasing crash risk.
Jeep is recalling certain 2018-2024 Wrangler and 2020-2024 Gladiator vehicles because the instrument panel cluster may fail due to an internal short circuit, preventing drivers from seeing the speedometer and warning lights.
Felling Trailers is recalling 2011-2022 Avtron D40548 trailers because the axle bracket may crack and break, allowing the axle to detach.
Beaver Visitec International is voluntarily recalling BVI CustomEyes Procedure Packs containing Sol-M syringes distributed nationwide. The recall affects 35 units with Part Number 584770 and is classified as FDA Class II.
OrthoPediatrics Canada is recalling FRT250 cartridges used in the Fassier-Duval Telescopic IM System because an incorrect component was substituted during assembly.
Stryker recalls iBur 3.0mm Precision Round surgical burs due to potential for excessive temperatures where the bur shank meets the bushing. Thermal injury risk may require medical intervention.
Beaver Visitec International recalls BVI CustomEyes Procedure Packs containing defective Sol-M syringes. About 1,756 units were distributed nationwide due to manufacturing defects.
Five Afinion 2 lab analyzers were distributed with incorrect configuration, potentially allowing waived laboratories to perform moderately complex assays that could produce erroneous results.
Beaver Visitec International voluntarily recalls BVI CustomEyes Procedure Packs containing syringes manufactured by Sol-Millennium Medical. The recall affects 351 units distributed nationwide.
Stryker recalled 1,226 iBur surgical burrs with multiple lot numbers worldwide due to potential overheating at the bur-shank connection point, which could cause tissue damage requiring medical intervention.
Stryker iBur 4.0mm precision surgical burs may overheat where the shank meets the distal bushing. Excessive heat could cause minor tissue damage or thermal injury requiring medical intervention.
Dr. Reddy's Laboratories is recalling IBU (Ibuprofen) 800 mg prescription tablets nationwide due to failed quality specifications. Testing found unknown impurities exceeding acceptable limits.