The Recall Desk

State

West Virginia product recalls

72,966 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 72,966 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

5676–5700 of 76507

  • ModerateFDA (Devices)·Z-2298-2025·2025-08-20

    Ultra IABP catheter kits carry indications not reviewed by the FDA

    Insightra Ultra IABP Catheter Kits are being recalled because the device carries indications and compatibility claims not reviewed by the FDA, and its instructions are inconsistent with product training.

    Product
    Brand Name: Ultra IABP Catheter Kit Product Name: Ultra IABP Catheter Kit Model/Catalog Number: IMU7F-40, IMU7F-35, IMU7F-30, IMU7F-25, and IMU7F-20 Software Version: Not applicable Product Description: The Insightra Ultra IABP Catheter Kit is a 7 French catheter available wi
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·H-0444-2025·2025-08-20

    Lithium orotate 5 mg product recalled after failing to meet labeled potency

    Lithium Orotate 5 mg distributed by Enjoy Nutrition, LLC is recalled nationwide for failing to meet its labeled potency, following a recall by the ingredient supplier.

    Product
    Lithium Orotate, 5MG, Distributed by Enjoy Nutrition, LLC. UPC#: 702730893968, 702730894064
    Category
    Food
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·H-0446-2025·2025-08-20

    Lithium orotate 20 mg product recalled after failing labeled potency testing

    Lithium Orotate 20 mg distributed by Enjoy Nutrition, LLC is recalled nationwide because it does not meet its labeled potency, following a recall by the ingredient supplier.

    Product
    Lithium Orotate, 20MG, Distributed by Enjoy Nutrition, LLC. UPC#: none
    Category
    Food
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2321-2025·2025-08-20

    Medication dispensing cabinets recalled after reports of delayed access during override workflow

    BD is recalling 6,076 Pyxis MedBank and MedBank Mini automated dispensing cabinets after reports of delayed access to medication caused by the override and Add Item workflow.

    Product
    Description/REF: BD PYXIS MEDBANK MINI 1FH-1FM/169-137, BD PYXIS MEDBANK MINI 4HM/169-113, BD PYXIS MEDBANK MINI 4HH/169-112, BD PYXIS MEDBANK MINI 3HH-1HM/169-111, BD PYXIS MEDBANK MINI 3HH-1FG/169-110, BD PYXIS MEDBANK MINI 2HM-1FM/169-109, BD PYXIS MEDBANK MINI 2HH-
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2292-2025·2025-08-20

    Bartels Legionella urinary antigen kits may contain particulate matter

    Bartels ELISA Legionella Urinary Antigen kits are being recalled because two lots have the potential to contain particulate matter. 968 kits are affected.

    Product
    Bartels ELISA Legionella Urinary Antigen. Model Number: B1029-440. In Vitro Diagnostic test kit for the presumptive diagnosis of past or current Legionnaires Disease.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereNHTSA·25V531000·2025-08-19

    Triumph Daytona 660 engines can fail from disrupted oil flow

    Triumph is recalling certain 2024-2025 Daytona 660 motorcycles because the engine may fail due to internal damage caused by a disruption of oil flow.

    Product
    TRIUMPH — TRIUMPH DAYTONA 660
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·25V530000·2025-08-18

    2026 RAM Trucks Instrument Panel Cluster Warning Light Malfunction

    Chrysler is recalling certain 2026 RAM 2500, 3500, 4500 Cab Chassis, and 5500 Cab Chassis vehicles because the instrument panel may display an incorrect brake system warning light, potentially failing to alert drivers to critical safety information.

    Product
    RAM — RAM 5500, 3500, 2500, 4500
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereCPSC·25435·2025-08-14

    Drinkmate one litre carbonation bottles can explode during use

    Drinkmate 1L Carbonation Bottles are being recalled because they can explode during use. Eight reports include four resulting in lacerations, impact injuries and hearing damage. About 106,200 units affected.

    Product
    Drinkmate 1L Carbonation Bottles
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereCPSC·25431·2025-08-14

    Werner Multi-Max Pro ladder locking mechanisms can jam without fully locking

    Werner 20' and 24' Multi-Max Pro multi-purpose ladders are being recalled because the locking mechanism can jam and not fully lock. Eighteen falls and fourteen injuries reported. About 122,250 units affected.

    Product
    Werner 20' and 24' Multi-Max Pro Multi-Purpose Ladders
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereCPSC·25432·2025-08-14

    Wolfgang Puck petite tea kettle infuser lids can fall off

    Wolfgang Puck Stainless Steel Petite Tea Kettles are being recalled because the infuser basket lid is loose and can fall off during use. Five of ten reports involved burns or scalding. About 40,000 units affected.

    Product
    Wolfgang Puck Stainless Steel Petite Tea Kettles
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereCPSC·25437·2025-08-14

    ESR HaloLock wireless power bank batteries can overheat and ignite

    ESR HaloLock wireless power banks are being recalled because the lithium-ion battery can overheat and ignite. Nine fires and explosions caused about $20,000 in property damage.

    Product
    ESR HaloLock Wireless Power Banks
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·25436·2025-08-14

    Viewrail floating stair LED modules can overheat and melt

    Electronic LED modules used with floating stairs and rails are being recalled because the module can overheat and melt, posing a fire hazard. About 2,720 units are affected.

    Product
    Electronic LED modules used on Floating Stairs and Rails
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·25433·2025-08-14

    Children's spiral tower toys contain small balls banned for toddlers

    Three-tiered spiral children's tower toys are being recalled because the toy contains small balls and is intended for children under three, violating the small ball ban. About 260 units affected.

    Product
    Children's Spiral Tower Toys
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·25434·2025-08-14

    Firefly Safe and Green fuel bottles have a non child-resistant applicator

    Firefly Safe & Green 32 oz fuel bottles are being recalled because the nozzle applicator is not child-resistant as required for hydrocarbons, and the fuel is incorrectly labeled "Non-Toxic".

    Product
    Firefly Safe & Green 32 oz. Fuel Bottles
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·25430·2025-08-14

    Remington hair dryers lack an immersion protection device against electrocution

    Remington brand hair dryers, model D3190DCDN, are being recalled because they lack an immersion protection device, posing a risk of electrocution or shock if dropped into water. About 56,300 units affected.

    Product
    Hair Dryers sold under the "Remington" brand, model number D3190DCDN
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-2129-2025·2025-08-13

    Plum Duo infusion system interface may become unresponsive during programming

    The Plum Duo Infusion System is being recalled because two sequences of programming events and alarm interactions may cause the user interface to become unresponsive. 4,677 units are affected.

    Product
    Plum Duo Infusion System, List Number: 400020401
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-2187-2025·2025-08-13

    BritePro Solo fiber optic laryngoscope handles may not illuminate properly

    BritePro Solo Single-Use Fiber Optic Laryngoscope Handles, REFs 040-310AU and 040-310U, are being recalled because the handles may not illuminate as intended.

    Product
    BritePro Solo Single-Use Fiber Optic Laryngoscope Handle Refs:040-310AU and 040-310U
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereNHTSA·25V526000·2025-08-13

    Volkswagen Tiguan rear axle tie rod bolts may be loose

    Volkswagen is recalling certain 2025 Tiguan vehicles because a tie rod bolt on the rear axle assembly may be loose, which can lead to a loss of vehicle control. 15 vehicles are affected.

    Product
    VOLKSWAGEN — VOLKSWAGEN TIGUAN
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-2179-2025·2025-08-13

    BD Alaris pump modules may perform outside established flow rate ranges

    BD Alaris Pump Module Model 8100 with Guardrails Suite MX software is being recalled because it may perform outside the established ranges for flow rate, bolus accuracy and occlusion alarm timing.

    Product
    BD Alaris Pump Module Model, 8100 with Guardrails, Suite MX software versions
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·H-0394-2025·2025-08-13

    Member's Mark freeze dried fruit packs tested positive for Listeria monocytogenes

    Member's Mark Freeze Dried Fruit Variety Pack 15 count is being recalled after the firm received positive test results for Listeria monocytogenes during routine testing. 21,552 boxes affected.

    Product
    Member's Mark FREEZE DRIED FRUIT VARIETY PACK 15 COUNT 5-0.35OZ (10g) STRAWBERRY POUCHES 5-0.42OZ (12g) BANANA POUCHES 5-0.25 OZ (10g) APPLE POUCHES NET WT 5.6OZ (160g) NO ADDED SWEETENERS ONE INGREDIENT ONLY PER PACK UPC 1 93968 50900 2
    Category
    Food
    Distribution
    44 states
  • SevereFDA (Devices)·Z-2183-2025·2025-08-13

    BritePro Solo laryngoscope handles and blades may not illuminate as intended

    BritePro Solo Single-Use Fiber Optic Handles and Blades in Macintosh and Miller sizes are being recalled because the handles may not illuminate as intended.

    Product
    BritePro Solo Single-Use Fiber Optic Handle and Blade Refs: 040-331U (Mac 1), 040-332U (Mac 2), 040-333U (Mac 3), 040-335U (Mac 3.5) 040-334U (Mac 4), 040-341U (Miller 1), 040-342U (Miller 2), 040-343U (Miller 3), 040-344U (Miller 4), 040-361U (Phillips 1), 040-36
    Category
    Medical Device
    Distribution
    Distributed nationwide