The Recall Desk

State

West Virginia product recalls

72,940 recalls have nationwide distribution and so reach West Virginia. 3,541 additional recalls listed West Virginia specifically in their distribution scope.

What the numbers show

Total
3,541
Critical
593
Severe
657
Most recent
2026-09-09

Of the 3,541 recalls naming West Virginia we have scored against our rubric, 593 (17%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 657 (19%) are Severe.

These figures cover only the 3,541 recalls whose distribution notice names West Virginia specifically. The 72,940 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

3376–3400 of 76481

  • HighCPSC·26249·2026-02-05

    LED Christmas headbands recalled over accessible button cell batteries

    About 250 Dresbe LED Christmas Headbands are being recalled because children can easily access the button cell batteries and the product lacks the warnings required by Reese's Law.

    Product
    Dresbe LED Christmas Headbands
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·26255·2026-02-05

    Ten drawer dressers recalled over tip-over and entrapment hazards

    About 5,000 EnHomee 10-Drawer Dressers are being recalled because they are unstable if not anchored to the wall, posing tip-over and entrapment hazards to children.

    Product
    EnHomee 10-Drawer Dressers
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·26238·2026-02-05

    Six drawer dressers recalled over tip-over and entrapment hazards

    About 600 Shintenchi 6-drawer dressers are being recalled because they are unstable if not anchored to the wall, posing tip-over and entrapment hazards to children.

    Product
    Shintenchi 6-Drawer Dressers
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·26247·2026-02-05

    Five drawer dressers recalled over tip-over and entrapment hazards

    About 50 Furnulem five-drawer dressers are being recalled because they are unstable if not anchored to the wall, posing tip-over and entrapment hazards to children.

    Product
    Furnulem 5-Drawer Dressers
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·26246·2026-02-05

    Kitosun submersible LED lights recalled over accessible coin batteries

    About 8,100 Kitosun Submersible LED Lights are being recalled because they contain lithium coin batteries that children can access easily and lack the warnings required by Reese's Law.

    Product
    Kitosun Submersible LED Lights
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·26V069000·2026-02-05

    2026 Hyundai Kona vehicles recalled for front steering knuckle defect

    Hyundai is recalling certain 2026 Kona vehicles because the front steering knuckles may crack and break due to a manufacturing error, which can cause loss of steering control and increase crash risk.

    Product
    HYUNDAI — HYUNDAI KONA
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·26241·2026-02-05

    Sixteen drawer dressers recalled over tip-over and entrapment hazards

    About 6,800 YITA 16-drawer dressers are being recalled because they are unstable if not anchored to the wall, posing tip-over and entrapment hazards to children.

    Product
    Little Cow Co. 9 oz candles in glass jars
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·26251·2026-02-05

    Soy wax candles recalled over glass jars that can crack

    About 1,140 Little Cow Co. 9 oz candles in glass jars are being recalled because the jar can crack or break during use.

    Product
    Yitahome, Uforic, Dextrus, Yintatech and ModFusion-branded Dressers
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·26229·2026-02-05

    Sweet birch essential oil recalled over bottles that are not child-resistant

    About 470 bottles of Lotus Joy Organic Sweet Birch Essential Oil are being recalled because the methyl salicylate they contain is not in child-resistant packaging.

    Product
    Lotus Joy Organic Sweet Birch Essential Oil Bottles
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·26V068000·2026-02-05

    Hyundai IONIQ battery bus bar may be improperly tightened

    Hyundai is recalling certain 2025-2026 IONIQ 5 and 2026 IONIQ 9 vehicles because the high voltage battery system may contain an improperly tightened bus bar, which can cause a short circuit.

    Product
    HYUNDAI — HYUNDAI IONIQ 9, IONIQ 5
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • CriticalFDA (Devices)·Z-1117-2026·2026-02-04

    Filled Broselow organizers recalled over potentially harmful dosing errors

    SunMed Holdings is recalling 89 units of the Filled Broselow Organizer, model 7730IALS, because the product contains potentially harmful dosing errors for Vecuronium, Flumazenil and Ketamine.

    Product
    Brand Name: Broselow Product Name: BROSELOW" FILLED BROSELOW ORGANIZER Model/Catalog Number: 7730IALS Software Version: Not Applicable Product Description: The Broselow Tape is a length- and weight-based reference tool specifically designed for pediatric emergency care. Comp
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • CriticalFDA (Devices)·Z-1114-2026·2026-02-04

    Pediatric emergency tapes recalled over potentially harmful drug dosing errors

    SunMed Holdings is recalling 95,300 units of the Broselow Pediatric Emergency Rainbow Tape because the product contains potentially harmful dosing errors for Vecuronium, Flumazenil and Ketamine.

    Product
    Brand Name: Broselow Product Name: Broselow Pediatric Emergency Rainbow Tape Model/Catalog Number: 7700REA Software Version: Not Applicable Product Description: The Broselow Tape is a length- and weight-based reference tool specifically designed for pediatric emergency care.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • CriticalFDA (Devices)·Z-1115-2026·2026-02-04

    Broselow Rainbow Tape 7700RE recalled over potentially harmful dosing errors

    SunMed Holdings is recalling 20,583 units of the Broselow Pediatric Emergency Rainbow Tape, model 7700RE, because it contains potentially harmful dosing errors for Vecuronium, Flumazenil and Ketamine.

    Product
    Brand Name: Broselow Product Name: Broselow Pediatric Emergency Rainbow Tape Model/Catalog Number: 7700RE Software Version: Not Applicable Product Description: The Broselow Tape is a length- and weight-based reference tool specifically designed for pediatric emergency care.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • CriticalFDA (Food)·H-0433-2026·2026-02-04

    Super greens powder tubs recalled over possible Salmonella Typhimurium contamination

    Superfoods, Inc. is recalling Live it Up brand Super Greens powder, net weight 8.5oz, because the products may be contaminated with Salmonella Typhimurium.

    Product
    Live it Up brand Super Greens; Chlorella, Spirulina, Wheatgrass, Kale, Broccoli, Spinach, Barley grass, Moringa, Parsley; Whole food dietary supplement powder; 30 day supply; NET WT. 8.5OZ (240G); Manufactured for Superfoods, Inc.; UPC: 860013190804 b.) Live it Up brand Super Gr
    Category
    Food
    Distribution
    Distributed nationwide
  • CriticalFDA (Food)·H-0434-2026·2026-02-04

    Super greens powder recalled over possible Salmonella Typhimurium contamination

    Superfoods, Inc. is recalling 795,834 units of Live it Up brand Super Greens because the products may be contaminated with Salmonella Typhimurium.

    Product
    a.) Live it Up brand Super Greens; Natural Wild Berry Flavor; Chlorella, Spirulina, Wheatgrass, Kale, Broccoli, Spinach, Barley grass, Moringa, Parsley; Whole food dietary supplement powder; 30 day supply; NET WT. 9.49oz (269.16g); Manufactured for Superfoods, Inc.; UPC: 86001319
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1181-2026·2026-02-04

    Condoms recalled over rodent activity in a distribution center

    Gold Star Distribution is recalling condoms over potential exposure of rodents and rodent activity in its distribution center.

    Product
    Condoms, labeled as: TROJAN MAGNUM CONDOMS 6/DSP BLACK, TROJAN LUBRICATED CONDOMS 6/DSP LITE BLUE, TROJAN SPERMICIDE CONDOMS 6/DSP DARK BLUE, TROJAN ULTRA THIN CONDOMS 6/DSP GREY, TROJAN RIBBED CONDOMS 6/DSP GOLD/BROWN, TROJAN NONLUBRICATED CONDOMS 6/DSP RED, TROJAN ULTRA HER
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighNHTSA·26V063000·2026-02-04

    Mercedes-Benz Tourrider Buses Recalled for Door Control Valve Defect

    Daimler Coaches is recalling 2026 Mercedes-Benz Tourrider buses because a faulty door valve may prevent doors from opening, delaying emergency evacuation.

    Product
    MERCEDES-BENZ — MERCEDES-BENZ TOURRIDER BUSINESS, TOURRIDER PREMIUM
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1205-2026·2026-02-04

    Evolution Upgrade 3.0T systems recalled over elastography stiffness value errors

    Philips North America is recalling 1 unit of the Evolution Upgrade 3.0T MR system because exported MR Elastography stiffness maps may show stiffness value errors.

    Product
    Evolution Upgrade 3.0T. Product Code (REF): 782143. MR systems with SW version R11.1 and R12.1.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1204-2026·2026-02-04

    Evolution Upgrade 1.5T systems recalled over elastography stiffness value errors

    Philips North America is recalling 3 units of the Evolution Upgrade 1.5T MR system because exported MR Elastography stiffness maps may show stiffness value errors.

    Product
    Evolution Upgrade 1.5T. Product Codes (REF): (1) 782148, (2) 782116. MR systems with SW version R11.1 and R12.1.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1179-2026·2026-02-04

    Q.namix R fluoroscopy systems recalled over unflipped and mismatched images

    Siemens is recalling 41 units of the LUMINOS Q.namix R fluoroscopic X-ray system because ortho images may not be flipped as preset and an image of a previous patient may be processed.

    Product
    Alphenix INFX-8000V, interventional fluoroscopic x-ray system
    Category
    Medical Device
    Distribution
    Distributed nationwide