The Recall Desk

State

Nevada product recalls

73,096 recalls have nationwide distribution and so reach Nevada. 5,696 additional recalls listed Nevada specifically in their distribution scope.

What the numbers show

Total
5,696
Critical
951
Severe
1,479
Most recent
2026-09-25

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.

These figures cover only the 5,696 recalls whose distribution notice names Nevada specifically. The 73,096 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

9626–9650 of 78792

  • SevereNHTSA·24V797000·2024-10-24

    GM diesel transmission control valves may fail and lock rear wheels

    GM is recalling certain 2020-2022 diesel Silverado, Sierra, Escalade, Tahoe, Suburban and Yukon vehicles because the transmission control valve may fail and cause rear wheel lock-up.

    Product
    CHEVROLET — CHEVROLET, GMC, CADILLAC TAHOE, SIERRA 3500, SILVERADO 2500, YUKON XL
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·24V796000·2024-10-24

    Inspire Recalls 2024 Newport Trailers Due to Cooktop Fire Risk

    Inspire RVs is recalling 2024 Newport 27 and 29 trailers because a cooktop circuit board may overheat and cause a fire. All affected units were repaired in September 2024.

    Product
    INSPIRE — INSPIRE NEWPORT 27, NEWPORT 29
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·24V798000·2024-10-24

    Nissan Z pedestrian sensor connectors may be reversed in the harness

    Nissan is recalling certain 2023-2024 Z vehicles because right-side pedestrian detection sensor connectors may be reversed, preventing the pop-up engine hood from activating.

    Product
    NISSAN — NISSAN Z
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·24V793000·2024-10-24

    Chrysler Pacifica side curtain airbag connectors may be improperly secured

    Chrysler is recalling certain 2020-2023 Pacifica and Voyager vehicles because an improperly secured side curtain airbag connector may prevent the airbags from deploying.

    Product
    CHRYSLER — CHRYSLER VOYAGER, PACIFICA
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·24V799000·2024-10-24

    Spartan Fire Recalls Fire Trucks Due to Cab Tilt Cylinder Defect

    Spartan Fire is recalling 2024-2025 fire trucks because a missing mechanical stop may allow the cab tilt cylinder to overextend, potentially causing the cab to drop.

    Product
    SPARTAN FIRE — SPARTAN FIRE, KME FC-94, PANTHER, METROSTAR, GLADIATOR
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·25019·2024-10-24

    CFMOTO 2024 CFORCE All-Terrain Vehicles Recalled for Throttle Failure Crash Hazard

    CFMOTO is recalling about 2,650 of its 2024 CFORCE 800 Touring and 2024 CFORCE 1000 Touring ATVs because the throttle lever can fail to return to idle, causing unexpected acceleration and crash risk. One minor injury has been reported.

    Product
    2024 CFORCE 800 Touring and 2024 CFORCE 1000 Touring All-Terrain Vehicles (ATVs)
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·24V800000·2024-10-24

    Orange EV Recalls T-Series and e-TRIEVER Trucks for Manual Errors

    Orange EV is recalling 2017-2024 T-Series and 2023-2024 e-TRIEVER trucks because manuals incorrectly describe the high-voltage lockout procedure, posing an electrical shock risk.

    Product
    ORANGE EV — ORANGE EV T-SERIES ELECTRIC TRUCK, E-TRIEVER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • ModerateCPSC·25020·2024-10-24

    PowerBlock Commercial Pro 100 Weight Sets with 5 lb Grip Handles Recalled

    PowerBlock is recalling about 1,845 Commercial Pro 100 weight sets sold with 5 lb grip handles because weight plates above 55 lbs can dislodge during use, posing an impact injury risk.

    Product
    Commercial Pro 100 sold with 5 lb grip handles
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereNHTSA·24E089000·2024-10-23

    Silver Eagle Recalls Eye and Shank Assemblies Due to Weld Fatigue

    Silver Eagle is recalling specific eye and shank assemblies because welds may crack, allowing the eye to separate from the trailer converter dolly and increasing crash risk.

    Product
    STRUCTURE:CRITICAL FASTENERS recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0012-2025·2024-10-23

    Atovaquone Oral Suspension Recalled for Cohnella Bacteria Contamination

    Bionpharma Inc. is recalling Atovaquone Oral Suspension (750 mg/5 mL) nationwide due to Cohnella bacteria contamination. The recall affects 1,980 bottles.

    Product
    ATOVAQUONE — ATOVAQUONE (ATOVAQUONE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-0035-2025·2024-10-23

    Enjoy Premium Taro Cookies recalled for undeclared milk allergen

    Enjoy Premium Taro Cookies contain undeclared milk allergen and were sold in Hawaii, Guam, and Nevada. Consumers with milk allergies should not consume this product.

    Product
    Enjoy Premium Taro Cookies packaged in 5.3 oz. foil pouches and 17.7 oz clear bags
    Category
    Food
    Distribution
    3 states
  • SevereFDA (Food)·F-0037-2025·2024-10-23

    Nuts.com recalls S'mores Bites for undeclared milk allergen

    Nuts.com is recalling S'mores Bites due to undeclared milk allergen. Milk chocolate was listed in the product description but omitted from the ingredient list, creating a labeling mismatch.

    Product
    S'mores Bites, 1 yummy pound, Distributed by Nuts.com, Cranford, NJ, 07016
    Category
    Food
    Distribution
    36 states
  • SevereFDA (Food)·F-0036-2025·2024-10-23

    Enjoy Premium Coconut Cookies Recalled for Undeclared Milk Allergen

    KTM Services, Inc. is recalling Enjoy Premium Coconut Cookies sold in Hawaii, Guam, Nevada, and online due to undeclared milk allergen. Consumers with milk allergies should not consume the product.

    Product
    Enjoy Premium Coconut Cookies packaged in 5.3 oz. foil pouches and 17.7 oz clear bags
    Category
    Food
    Distribution
    3 states
  • HighFDA (Devices)·Z-0131-2025·2024-10-23

    Rolling Walker Backrest May Disengage During Position Changes Creating Fall Risk

    Nova Ortho-Med is recalling 1,585 MONARCH ROLLATOR RED units because the backrest may disengage from its holder when users adjust from a slouched to upright position, creating a fall hazard.

    Product
    Brand Name: NOVA ORTHO-MED INC. Product Name: MONARCH ROLLATOR RED Model/Catalog Number: 4329RD Product Description: ROLLING WALKER MOBILITY AID
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighNHTSA·24V790000·2024-10-23

    Volvo trucks with Bendix EC80 units may lose safety system functions

    Volvo Trucks is recalling certain 2020-2025 trucks with Bendix EC80 Advanced Electronic Control Units because electrical noise may cause the ECU to misprocess commands or stop working.

    Product
    VOLVO — VOLVO VNRE (ELECTRIC), VAH, VHD, VN
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0068-2025·2024-10-23

    BlueFIRE Inflation Device Recalled for Sterile Barrier Defect Risk

    BlueFIRE Inflation Devices may have a small hole in the sterile barrier, potentially exposing patients to pathogens that could cause infection. Contact your healthcare provider if you received this device.

    Product
    BlueFIRE Inflation Device, REF: IN10140
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0049-2025·2024-10-23

    KINOVA Jaco assistive robot recalled for potential fire hazard

    Kinova Inc is recalling 949 KINOVA Jaco assistive robots due to a potential fire hazard that may occur if a damaged robot arm interacts with a wheelchair exhibiting electrical leakage.

    Product
    KINOVA Jaco assistive robot. Model Numbers: PJ 0000 0001, PJ 0000 0012, PJ 0090 0001, PJ 0090 0006, KR MJ2 0001. Jaco replaces the function of the upper limb on one side of the body.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0090-2025·2024-10-23

    Leica Biosystems Cryostat Model CM3050 S lacks warning label for flammable sprays

    Leica cryostat units lack a warning about flammable freezing sprays that can ignite in the chamber. The company discovered through post-market surveillance that users were applying these flammable sprays without being warned of the fire hazard.

    Product
    Leica Biosystems Cryostat Model Number CM3050 S, Material Numbers: a) 14047033518, b) 14903050S01, c) 14903050S02, d) 14903050S03; for freezing and sectioning tissue samples
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0009-2025·2024-10-23

    Duloxetine 20mg Delayed-Release Capsules Recalled for N-Nitroso Impurity

    Breckenridge Pharmaceutical is recalling 7,107 bottles of Duloxetine 20mg delayed-release capsules nationwide due to N-nitroso-duloxetine impurity exceeding FDA interim limits. No illnesses have been reported.

    Product
    DULOXETINE — DULOXETINE (DULOXETINE HYDROCHLORIDE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0085-2025·2024-10-23

    Leica Cryostat Model CM1100 Recalled for Fire Risk from Flammable Freezing Sprays

    Leica Biosystems recalls its Cryostat Model CM1100 due to inadequate warnings about using flammable freezing sprays, which can ignite and cause serious injuries. The device labeling lacked required safety warnings prior to 2019.

    Product
    Leica Biosystems Cryostat Model Number CM1100, Material Number 14046931130, for freezing and sectioning tissue samples
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0072-2025·2024-10-23

    basixTOUCH Inflation Device May Have Sterile Barrier Defect

    Merit Medical Systems is recalling basixTOUCH Inflation Devices due to a potential hole in the sterile barrier. The defect may expose patients to pathogens and pyrogens, increasing infection risk.

    Product
    basixTOUCH Inflation Device, REF: IN8130/JPC, IN8152/C, IN8302/C, IN8352/C, IN8802/C, IN8130/C, IN8130/C
    Category
    Medical Device
    Distribution
    Distributed nationwide