The Recall Desk

State

Nevada product recalls

72,933 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
2026-09-09

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.

These figures cover only the 5,692 recalls whose distribution notice names Nevada specifically. The 72,933 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

2776–2800 of 78625

  • HighFDA (Devices)·Z-1585-2026·2026-03-25

    Stago D-dimer assay shows positive bias across entire analytical range

    Diagnostica Stago is recalling the STA Liatest D-Di kit after investigations confirmed a positive bias in D-dimer measurements throughout the entire analytical range.

    Product
    Brand Name: STA Liatest D-Di Product Name: STA Liatest D-Di Model/Catalog Number: REF 00515 Product Description: in vitro diagnostic. The STA - Liatest D-Di kit is an assay for the quantitative determination of D-dimer in venous plasma for use on STA-R, STA Compact and STA Sat
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1572-2026·2026-03-25

    Stryker sagittal saw attachment cover screws may loosen and detach

    Howmedica Osteonics is recalling the MICS3 Angled Sagittal Saw Attachment because the external screws securing the cover to the saw housing may loosen and detach during use.

    Product
    MICS3 Angled Sagittal Saw Attachment; Part Number: 210490
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·H-0579-2026·2026-03-25

    Clover Sonoma Cottage Cheese Recalled for Potential Under-Pasteurization

    Clover Sonoma low-fat cottage cheese (16 oz and 32 oz sizes) is being recalled due to potential under-pasteurization from a broken pasteurizer seal. The product may not be safe for consumption.

    Product
    CLOVER SONOMA COTTAGE CHEESE LOW FAT 2% MILKFAT NET WT 16OZ UPC 0 70852 54400 7 & 32OZ UPC 0 70852 54200 3 DISTRIBUTED BY: CLOVER-STORNETTA FARMS LLC PETALUMA, CA 94952
    Category
    Food
    Distribution
    11 states
  • HighFDA (Drugs)·D-0407-2026·2026-03-25

    Brimonidine and timolol eye drops recalled over sterility assurance failure

    Apotex is recalling two lots of Brimonidine Tartrate/Timolol Maleate Ophthalmic Solution for lack of assurance of sterility.

    Product
    BRIMONIDINE TARTRATE/TIMOLOL MALEATE OPHTHALMIC SOLUTION — BRIMONIDINE TARTRATE/TIMOLOL MALEATE OPHTHALMIC SOLUTION (BRIMONIDINE TARTRATE AND TIMOLOL MALEATE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1581-2026·2026-03-25

    Leksell Gamma Knife recalled over adapter not properly aligned or locked

    Elekta is recalling Leksell Gamma Knife radiosurgery systems, covering the Perfexion, Icon and Elekta Esprit models, due to an adapter not being properly aligned or locked in place.

    Product
    Brand Name: Leksell Gamma Knife Product Description: Leksell Gamma Knife¿ Perfexion Leksell Gamma Knife¿ Icon" Leksell Gamma Knife¿ Elekta Esprit Leksell Gamma Knife¿ (available models Elekta Esprit, Icon", and Perfexion") is a radiosurgery system for use in the stereot
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1565-2026·2026-03-25

    Abbott ID NOW influenza test lot shows higher invalid result rates

    Abbott is recalling one lot of the ID NOW Influenza A & B 2 test after confirming the lot has a higher occurrence of invalid rates than stated in the Instructions for Use.

    Product
    Product Name: ID NOW" Influenza A & B 2 Model/Catalog Number: 427-000 Software Version: Not Applicable Product Description: Influenza A/B virus nucleic acid IVD, kit, nucleic acid technique Component: Not Applicable
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0398-2026·2026-03-25

    Dexamethasone injection failed impurity specifications at product expiry testing

    Somerset Therapeutics is recalling one lot of Dexamethasone Sodium Phosphate Injection after out-of-specification impurity results at product expiry during long term stability testing.

    Product
    DEXAMETHASONE SODIUM PHOSPHATE — DEXAMETHASONE SODIUM PHOSPHATE (DEXAMETHASONE SODIUM PHOSPHATE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1583-2026·2026-03-25

    ConvaTec EsteemBody drainable pouch REF 423653 may leak

    ConvaTec is recalling one lot of the EsteemBody Drainable Pouch, REF 423653, because the drainable large pouch may leak due to a manufacturing issue.

    Product
    Convatec, EsteemBody Drainable Pouch REF:423653 10-35mm
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1574-2026·2026-03-25

    Artegraft vascular graft recalled over incorrect lot outer packaging labeling

    LeMaitre Vascular is recalling one Artegraft Vascular Graft, REF AG740, because of a labeling mix-up resulting in the incorrect lot outer packaging of the product.

    Product
    Artegraft Vascular Graft; REF#: AG740;
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1587-2026·2026-03-25

    Cardiosave battery charging station left bay screw prevents full battery insertion

    Datascope is recalling the Battery Charging Station, model 0998-00-0802, because a protruding screw in the left battery bay limits full insertion of certain batteries and prevents proper charging.

    Product
    Battery Charging Station; Model: 0998-00-0802;
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1580-2026·2026-03-25

    Stryker Cub pediatric cribs sold in USA missing two warning labels

    Stryker is recalling Cub Pediatric Cribs, model FL19H, because cribs sold in the USA are missing two access door warning labels.

    Product
    Cub Pediatric Crib, Model FL19H
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereNHTSA·26V182000·2026-03-24

    Nova Bus driver seat belt tension device may not disengage

    Nova Bus is recalling certain 2016-2023 LFS and LFS Artic transit buses because the driver's seat belt tension-relieving device may fail to disengage without manual intervention. This fails FMVSS 208.

    Product
    NOVA BUS — NOVA BUS LFS, LFS ARTIC
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·26V180000·2026-03-24

    Lexus LX Recall: Front Passenger Air Bag May Deploy Improperly

    Toyota is recalling 2022-2024 Lexus LX vehicles because a seat frame issue may cause the front passenger air bag to deploy incorrectly during a crash.

    Product
    LEXUS — LEXUS LX
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • ModerateNHTSA·26V179000·2026-03-24

    2024–2026 Toyota and Lexus vehicles load carrying capacity label incorrect

    Toyota is recalling certain 2024–2026 Toyota and Lexus vehicles because the load carrying capacity modification label may display inaccurate added weight values. Vehicles with incorrect maximum capacity weight may be overloaded, increasing crash risk.

    Product
    TOYOTA — TOYOTA, LEXUS RAV4 HYBRID, TACOMA HYBRID, GRAND HIGHLANDER, CROWN SIGNIA
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·26V177000·2026-03-23

    Winnebago motorhome front turn signal lenses are smaller than required

    Winnebago is recalling certain 2017-2022 Brave, Itasca Sunova, Adventurer and Sunstar motorhomes because the front turn signals may have a smaller than required luminous lens area. This fails FMVSS 108.

    Product
    WINNEBAGO — WINNEBAGO, ITASCA ADVENTURER, BRAVE, SUNSTAR, SUNOVA
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·26V174000·2026-03-20

    Grand Design motorhome steps may deploy unexpectedly while in transit

    Grand Design is recalling certain 2025-2026 Lineage motorhomes because the entry door position switch may not read that the door is closed, allowing the steps to deploy unexpectedly.

    Product
    GRAND DESIGN — GRAND DESIGN LINEAGE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·26V172000·2026-03-20

    Mercedes-Benz Recalls 2026 GLC Models for Rear Seat Belt Defect

    Mercedes-Benz is recalling 2026 GLC models because the center rear seat belts may lack the child seat protection function, increasing injury risk in a crash.

    Product
    MERCEDES-BENZ — MERCEDES-BENZ GLC 300 4MATIC COUPE, GLC 300, GLC 300 4MATIC, AMG GLC43 4MATIC
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·26V170000·2026-03-20

    Altec Recalls 2025 Cranes and Derricks Due to Missing Lighting Harness

    Altec is recalling 2025 AC Series Cranes and Digger Derricks because a missing harness may cause loss of body or trailer lights, increasing crash risk.

    Product
    ALTEC — ALTEC AC SERIES CRANE, DIGGER DERRICK
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·26V171000·2026-03-20

    Braun Recalls 2023-2024 Ram ProMaster Vehicles Due to Window Glass Defect

    Braun is recalling 2023-2024 Ram ProMaster vehicles because the installed window may have the wrong type of glass for an emergency exit, increasing the risk of ejection and injury during a crash.

    Product
    BRAUN — BRAUN RAM PROMASTER
    Category
    Vehicle
    Distribution
    Distributed nationwide