State
73,198 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 73,198 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
Kubota is recalling about 3,170 RTV-XG850 Sidekick utility vehicles sold between March 2023 and September 2023 due to improper steering shaft assembly that could cause loss of control and crash hazards.
Empower Brands is recalling about 319,000 PowerXL DUAF-10 and DUAF-005 Vortex Dual-Basket Air Fryers because the plastic U-Channel connector can break during use, posing a burn hazard. The firm has received 41 reports of breakage, including three burn injuries.
WeatherBeeta USA is recalling about 2,300 Collegiate English horse-riding saddles because the rivet or stirrup bar can break, causing the rider to fall. One fall injury has been reported.
BRP is recalling about 14,555 Model Year 2022 and 2023 Can-Am Commander, Defender, and Maverick Trail side-by-side vehicles because the operator's guide contains incorrect maintenance intervals for the clutch, which can lead to clutch failure and fragment ejection, posing a risk of serious injury.
Polaris is recalling Model Year 2023-2024 Ranger XP Kinetic recreational off-road vehicles because pressing the brake and throttle pedals together can deactivate the throttle, creating a crash hazard when the brake is released.
Daimler Trucks North America is recalling 2021-2025 Thomas Built SAF-T-LINER C2 Jouley electric school buses because a high voltage inverter cable may not be secured properly, potentially causing a loss of drive power.
Vornado Air LLC is recalling approximately 1.75 million Steamfast Home & Away Travel Steam Irons because the power cord can become damaged near the bushing, posing fire, burn, and electrical shock hazards.
Savvy Rest is recalling about 84 quilted cotton mattress pads because they fail to meet the federal flammability standard for mattress pads and pose a fire hazard. No injuries have been reported.
Traeger is recalling about 37,000 Flatrock Flat Top Propane Grills because burner control knobs can be incorrectly labeled, allowing the grill to be unintentionally left on and posing a fire hazard. No fires or injuries have been reported.
Novartis Pharmaceuticals is recalling SANDIMMUNE Oral Solution (cyclosporine 100 mg/mL) due to crystallization found in bottles. The affected lots were distributed nationwide.
Daimler Trucks North America is recalling 321 Thomas Built school buses because a rear interior joint may be too weak, increasing injury risk in a crash.
B. Braun Infusomat Administration Sets may have incorrect tubing dimensions that cause false air-in-line alarms, interrupting medication delivery. The defects may prevent critical medications from reaching patients.
The FDA is recalling CARDIOHELP Emergency Drive units due to potential blocking that impairs blood flow. Affected patients may experience ischemia and hypoxia from inappropriate low blood oxygen.
Dr. Ergin's SugarMD glucose support capsules are recalled nationwide because they were marketed without FDA approval and are contaminated with the pharmaceutical ingredients metformin and glyburide. Approximately 32,117 units were distributed in the U.S.
Freshpoint Of Southern Ca is recalling Imperial Fresh whole cantaloupes (3ct and 6ct) distributed to food services in California, Arizona, and Nevada due to possible Salmonella contamination.
Staar Surgical Company is recalling 9 EVO VISIAN intraocular lenses due to potential specification non-compliance. The affected devices were distributed to 40 US states.
Staar Surgical recalls 51 EVO+VISIAN intraocular lenses due to potential specification non-compliance. Affected devices were distributed across multiple U.S. states.
STAQ Pharma is recalling ROPivacaine HCl 0.2% injection bags nationwide due to leaking bags caused by manufacturing quality control failures. No illnesses or injuries have been reported.
Randox is recalling RANDOX Total Bilirubin reagent because reports indicate elevated patient results when using plasma samples with this reagent.
Stryker ProCuity beds (model 3009) are missing electrical safety test values, presenting risks of electrical shock and tissue burns. FDA Class II recall.
Stryker's ProCuity bed series model 3009 lacks required electrical safety test documentation, creating a risk of tissue burns or electrical shock. The beds are distributed across North America, Europe, and other regions.
Integra LifeSciences is recalling 510 units of Cranial Access Kits due to a defect in outer packaging that can split spontaneously, compromising device sterility and increasing infection risk in neurosurgery.
IHB Operations is recalling Freedom Boom ceiling-mounted equipment dispensers due to weakened connection points on the suspension arm that could cause equipment failure. The defect affects 1,497 units distributed across multiple US states.
CooperSurgical H/S Catheter Sets may have defective bonding material causing component detachment or leakage. The sets are used in hysterosalpingography procedures to detect uterine abnormalities.
Integra LifeSciences is recalling 180 Cranial Access Kits due to a packaging defect that can cause splits, compromising the sterility of the surgical device.