The Recall Desk

State

Nevada product recalls

72,820 recalls have nationwide distribution and so reach Nevada. 5,692 additional recalls listed Nevada specifically in their distribution scope.

What the numbers show

Total
5,692
Critical
951
Severe
1,476
Most recent
2026-09-02

Of the 5,692 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 1,476 (26%) are Severe.

Which agencies issued them

These figures cover only the 5,692 recalls whose distribution notice names Nevada specifically. The 72,820 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

726–750 of 78512

  • ModerateFDA (Drugs)·D-0664-2026·2026-07-15

    Methohexital Sodium 100 mg/10 mL Compounded Drug Recalled Nationwide

    QuVa Pharma is recalling Methohexital Sodium 100 mg/10 mL compounded drug vials due to failed impurities and degradation specifications. The recall affects multiple lot numbers distributed nationwide.

    Product
    Methohexital Sodium, 100 mg/10 mL (10 mg/mL), Total Volume: 10 mL, Rx only, Compounded drug, QuVa Pharma, 1075 W Park One Dr, Suite 100, Sugar Land, TX 77478, Product code: 70092-1310-46.
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2677-2026·2026-07-15

    Aquacel Ag Surgical SP Surgical Dressing Recalled for Out-of-Specification Thickness

    ConvaTec is recalling Aquacel Ag Surgical SP dressings (Lot 5G00809) that were manufactured with greater-than-specified thickness. The dressing is used in surgical wound care.

    Product
    Aquacel Ag Surgical SP REF: 413556 9cm x 15cm/3.5 in. x 6 in., Sterile R
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2676-2026·2026-07-15

    Olympus Single Use Distal Cover MAJ-2315 Duodenovideoscope Replacement

    Olympus Corporation of the Americas is replacing the previous design of its Single Use Distal Cover (MAJ-2315) with a newly designed version for use with EVIS EXERA III Duodenovideoscopes.

    Product
    Olympus Single Use Distal Cover, Catalog Number MAJ-2315, Used with: EVIS EXERA III Duodenovideoscope TJF-Q190V- designed to be attached to Olympus duodenovideoscopes to cover the distal end of the insertion tube and around the forceps elevator; duodenoscope and accessories, flex
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2714-2026·2026-07-15

    OmniTract Surgical Retractor System sterilization instructions require extended dry time

    Integra LifeSciences is recalling the OmniTract Surgical Retractor System because the sterilization instructions require a longer dry time than stated in the current manual. The dry time must be extended to 90, 110, or 120 minutes depending on the sterilization cycle used.

    Product
    OmniTract Surgical Retractor System, which includes 633 of the firm s product codes.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0666-2026·2026-07-15

    Gasco Isopropyl Alcohol 70% recalled nationwide for subpotency

    Gasco Industrial Corp. is recalling Gasco Isopropyl Alcohol 70% (1 US Gallon) nationwide due to subpotency. The voluntary recall affects specific lot numbers manufactured before the expiration date.

    Product
    Gasco Isopropyl Alcohol 70%, Net Contents: 1 US Gallon (3.78 L), Manufactured by: Gasco Industrial Corp., PO Box 1360, Gurabo, PR 00778, Made in USA
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0670-2026·2026-07-15

    Drogueria San Juan Isopropyl Alcohol 70% recalled for subpotency

    Gasco Industrial Corp. is recalling Drogueria San Juan Puerto Rico Isopropyl Alcohol 70% (32 oz.) due to subpotency. Affected lots 250206B1, 250218B2, and 250507B1 were distributed nationwide in the US.

    Product
    Drogueria San Juan Puerto Rico Isopropyl Alcohol 70%, 32 oz., 946 mL, Distributed by: Drogueria San Juan, Calle De Diego 590, Sabana Llana Rio Piedras, PR 00924, UPC 659685696567.
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereNHTSA·26E046000·2026-07-14

    Ford Recalls Integrated Trailer Brake Control Kits for F-150s

    Ford is recalling specific integrated trailer module accessory kits for 2021-2026 F-150s because they may lose communication, causing a loss of trailer brakes and lights.

    Product
    ELECTRICAL SYSTEM: INTEGRATED TRAILER BRAKE CONTROL recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·26V450000·2026-07-14

    Winnebago Recalls 2027 Navion and View RVs for Fire Risk

    Winnebago is recalling 2027 Navion and View recreational vehicles because a rooftop fan circuit board may overheat and cause a fire.

    Product
    WINNEBAGO — WINNEBAGO VIEW, NAVION
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·26V452000·2026-07-14

    2026 Hyundai Kona rear center seat belt buckle failure risk

    Hyundai is recalling certain 2025 Kona Electric and 2026 Kona vehicles because the rear center seat belt buckle may fail to properly restrain an occupant during a crash. Dealers will replace the buckle assembly for free.

    Product
    HYUNDAI — HYUNDAI KONA, KONA ELECTRIC
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·26V446000·2026-07-10

    Grand Design Lineage RVs Recalled for Rooftop Fan Fire Risk

    Grand Design is recalling 2026-2027 Lineage RVs because a rooftop fan component may overheat and cause a fire. Dealers will replace the part free of charge.

    Product
    GRAND DESIGN — GRAND DESIGN LINEAGE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·26E045000·2026-07-10

    Tenneco Recalls NAPA Steering Inner Tie Rod Ends for Ford Vehicles

    Tenneco Automotive is recalling NAPA steering inner tie rod ends for certain Ford C-Max, Escape, and Focus models because the stud may separate, causing a loss of steering.

    Product
    STEERING:LINKAGES:TIE ROD ASSEMBLY recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereCPSC·26608·2026-07-09

    Moodooy Adult Portable Bed Rails Recalled for Entrapment and Asphyxiation Risk

    Moodooy Adult Portable Bed Rails sold on Amazon violate mandatory safety standards and pose risk of entrapment and asphyxiation. The rails lack required warning labels and users can become trapped within the rail or between the rail and mattress.

    Product
    Moodooy Adult Portable Bed Rails
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereNHTSA·26V444000·2026-07-09

    2026 Volvo VNL, VNR, VHD, VN, VAH trucks recalled for loose steering

    Volvo Trucks is recalling certain 2026 VNL, VNR, VHD, VN, and VAH vehicles because the steering arm may not be tightly fastened to the steering knuckle, risking loss of steering control and crashes.

    Product
    VOLVO — VOLVO VHD, VN, VNR (4), VAH
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereCPSC·26610·2026-07-09

    Flaunt MagSafe Battery Chargers Recalled for Fire and Burn Hazards

    About 1,400 Flaunt MagSafe Battery Chargers (model E33A) are being recalled because the lithium-ion battery can overheat and ignite. The company has received five reports of the power banks catching fire, including two reports of burns and four reports of property damage.

    Product
    Flaunt MagSafe Battery Chargers
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·26609·2026-07-09

    WonderStone Infant Walkers Recalled for Fall Hazard Risk

    WonderStone Infant Walkers sold on Walmart.com violate mandatory infant-walker standards because they can fit through doorways and fail to stop at steps, posing a risk of serious injury or death from falls. No injuries have been reported.

    Product
    WonderStone Infant Walkers
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·26606·2026-07-09

    Insignia Front Control Gas Ranges Recalled for Fire Hazard Risk

    Best Buy is recalling about 3,820 Insignia Front Control Gas Ranges because the front-mounted knobs can be accidentally activated by humans or pets, creating a fire hazard risk.

    Product
    Insignia Front Control Gas Ranges
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·26611·2026-07-09

    Kobalt 24V and 48V Yard Power Tools with USB-C Batteries Recalled for Fire Risk

    Greenworks Tools recalls Kobalt yard power tools with USB-C batteries due to risk of fire when batteries are charged via the USB-C port while inserted in the tool. The firm received 34 reports of batteries smoking, sparking, or catching fire, with no injuries reported.

    Product
    Kobalt 24V and 48V Trimmers, Blowers, Mowers, Chainsaws and Pruning Saws with USB-C Batteries
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·26605·2026-07-09

    Cuisinart Propel Four Burner Gas Grill Recalled Due to Laceration Hazard

    Conair is recalling the Cuisinart Propel+ Four Burner 3-in-1 Gas Grill because the tempered glass window in the pizza oven can shatter during use, posing a laceration risk. About 12,660 units were sold.

    Product
    Cuisinart Propel+ Four Burner 3-in-1 Gas Grill with pizza oven
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·26607·2026-07-09

    Biometric Firearm Safes Recalled Due to Unauthorized-Access Hazard

    BBRKIN and MouTec biometric firearm safes can be opened by unauthorized users, creating a serious injury and death risk. Consumers should immediately stop using the biometric feature and use the key only.

    Product
    BBRKIN and MouTec Biometric Firearm Safes
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • CriticalFDA (Devices)·Z-2604-2026·2026-07-08

    Omnipod DASH Pod insulin pump affected by external cannula damage

    Insulet Corporation is recalling Omnipod DASH Pods worldwide due to external soft cannula damage during manufacturing that can cause insulin to leak around the pod instead of being delivered. This may lead to high blood glucose levels and, in severe cases, diabetic ketoacidosis or death.

    Product
    Omnipod DASH Pod. Includes the below Model/REF Numbers: 1. POD-BLE-I1-525 (5-Pack), POD-BLE-I1-520 (Single Pod). 2. POD-BLE-I1-529 (10-Pack), POD-BLE-I1-520 (Single Pod). 3. BLE-I1-529 (10-Pack), BLE-I1-520 (Single Pod). 4. BLE-C1-529 (10-Pack), BLE-C1-520 (Single
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-2615-2026·2026-07-08

    Reprocessed Electrophysiology Catheters Recalled for Residual Particles

    Medline Industries is recalling reprocessed electrophysiology and ultrasound catheters with residual particles that may cause inflammation, infection, or blood clots if contacted with blood or the heart.

    Product
    Reprocessed Electrophysiology Catheters and Ultrasound Catheters Item no. 401206RH, St. Jude Medical Response" Diagnostic Electrophysiology Catheter 4 Elec. 10mm; Item no. 401305RH, St. Jude Medical Response" Diagnostic Electrophysiology Catheter 10 Elec. 2-5-2mm.
    Category
    Medical Device
    Distribution
    Distributed nationwide