State

West Virginia product recalls

72,984 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.

Which agencies issued them

These figures cover only the 3,541 recalls whose distribution notice names West Virginia specifically. The 72,984 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

6626–6650 of 76525

ModerateFDA (Devices)·Z-1745-2025·2025-05-21
Contour Gold Eyelid Weight implants recalled for mislabeling
Meddev Corp is recalling Contour Gold Eyelid Weight implants (Model LL3012) due to mislabeling. Thirty-four weights distributed nationwide are affected.
Product
Brand Name: Contour Product Name: Contour Gold Eyelid Weight Model/Catalog Number: LL3012 Product Description: Contour Gold Eyelid Weight, 1.2 gm MedDev Contour and ThinProfile Eyelid Weight Implants are designed for the gravity-assisted treatment of protracted permanent
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1765-2025·2025-05-21
Centurion Sterile Weitlaner Retractor recalled for packaging puncture risk
Medline Industries is recalling Centurion Sterile Weitlaner Retractors (2,100 units) due to potential puncture damage to sterile packaging. The defect could compromise the sterility of the surgical instrument.
Product
Centurion Sterile Weitlaner Retractor, Reorder: 67315
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0417-2025·2025-05-21
La Roche-Posay Effaclar Duo Acne Treatment Recalled for Benzene Contamination
La Roche-Posay Effaclar Duo acne treatment is being recalled due to detected trace levels of benzene. The recall affects 2,226,801 units distributed nationwide.
Product
La Roche-Posay Laboratoire Dermatologique Effaclar Duo Dual Action Acne Treatment, 5.5% Benzoyl Peroxide Acne Medication, 40 mL (135 FL. OZ.) Tube per carton, La Roche-Posay LLC, 10 Hudson Yards, New York, NY 10001, La Roche-Posay, Laboratoire Dermatologique, CAI 86270, La Roche-
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1747-2025·2025-05-21
FoundationOne Companion Diagnostic reports clinically relevant variants requiring amendment
Foundation Medicine is recalling four FoundationOne Companion Diagnostic (F1CDx) test reports sent to customers that contained clinically relevant variants requiring amendment, including one with an incorrect negative companion diagnostic claim.
Product
FoundationOne Companion Diagnostic (F1CDx)
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1741-2025·2025-05-21
Halyard CHRIST SUTURE KIT surgical needles coating defect recall
AVID Medical is recalling Halyard CHRIST SUTURE KIT units due to a raw material issue in the needle coating that may cause silicone to be removed during use, potentially affecting surgical performance.
Product
Halyard CHRIST SUTURE KIT. General Procedure Tray Convenience Kit
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1742-2025·2025-05-21
Halyard SUTURE PACK CABG Cardiovascular Kit Needle Coating Issue
AVID Medical is recalling Halyard SUTURE PACK CABG Cardiovascular Procedure Convenience Kits due to a raw material defect in the surgical needle coating that may reduce needle performance or cause coating removal during use.
Product
Halyard SUTURE PACK CABG. Cardiovascular Procedure Convenience Kit.
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1764-2025·2025-05-21
CMS8000 Patient Monitor Has Nine Cybersecurity Vulnerabilities
The CMS8000 Patient Monitor manufactured by Contec Medical Systems Co., Ltd. has nine identified cybersecurity vulnerabilities. The FDA is issuing this Class II recall affecting approximately 7,773 units distributed nationwide.
Product
CMS8000 Patient Monitor
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1761-2025·2025-05-21
Augmedics Perc Pin Adaptor component recalled due to design defect
Augmedics Ltd. is recalling the Perc Pin Adaptor, a component of the xvision Spine surgical navigation system, because the tightening knob is inconvenient to use and the tightening markings are improperly placed.
Product
Augmedics Perc Pin Adaptor, Model/Catalog Number AMCH07200, a component of the xvision Spine (XVS) system, an image-guided navigation system that is designed to assist surgeons in placing pedicle screws accurately, during open or percutaneous computer-assisted spinal surgery.
Category
Medical Device
Distribution
Distributed nationwide
HighNHTSA·25V327000·2025-05-20
Braun Recalls Demers Ambulances Due to Unsecured Cushion Equipment Storage
Braun Industries is recalling specific Demers ambulance models because improperly installed cushion equipment storage may allow items to detach during transit, increasing injury risk.
Product
DEMERS — DEMERS, DEMERS AMBULANCES TSE, MX164E, MXP150E, TXE
Category
Vehicle
Distribution
Distributed nationwide
HighNHTSA·25V328000·2025-05-20
Orange EV Recalls Electric Trucks Due to Obstructed Backup Lights
Orange EV is recalling specific electric trucks because a pintle hook blocks the backup lights, reducing visibility and increasing crash risk.
Product
ORANGE EV — ORANGE EV E-TRIEVER, HUSK-E, T-SERIES ELECTRIC TRUCK
Category
Vehicle
Distribution
Distributed nationwide
SevereNHTSA·25T008000·2025-05-19
Michelin Recalls Agilis Cross Climate Tires Due to Tread Rubber Detachment
Michelin is recalling specific Agilis Cross Climate tires because chunks of tread rubber may detach, increasing the risk of tire failure and a crash.
Product
TIRES:TREAD/BELT recall
Category
Vehicle
Distribution
Distributed nationwide
SevereNHTSA·25V319000·2025-05-16
Isuzu Recalls 2025 NRR EV Due to Electrical Overheating Risk
Isuzu is recalling 2025 NRR EV vehicles because a gap in the electrical system may cause overheating and loss of drive power, increasing crash risk.
Product
ISUZU — ISUZU NRR EV
Category
Vehicle
Distribution
Distributed nationwide
CriticalCPSC·25285·2025-05-15
Chill Pill Magnetic Haptic Fidget Toys recalled due to ingestion hazard
FidgetThings is recalling Chill Pill Magnetic Haptic Fidget Toys Red Bumpy because they violate federal magnet regulations and pose a risk of serious injury or death if swallowed by children.
Product
Chill Pill Magnetic Haptic Fidget Toys Red Bumpy
Category
Consumer Product
Distribution
Distributed nationwide
SevereCPSC·25286·2025-05-15
Child Safety Gates Recalled for Entrapment and Fall Hazards
Multiple child safety gates sold on Amazon.com violate federal safety regulations, posing risk of serious injury or death from entrapment and falls. Consumers should stop using the gates immediately and contact the seller for disposal and refund.
Product
Child Safety Gates
Category
Consumer Product
Distribution
Distributed nationwide
SevereCPSC·25279·2025-05-15
NICREW Submersible RGB LED Lights Recalled for Coin Battery Ingestion Hazard
NICREW 15" Submersible RGB LED Lights with remote controls are recalled because the remote's lithium coin battery can be easily accessed by children, creating a serious ingestion hazard that can cause internal burns and death.
Product
NICREW 15" Submersible RGB LED Lights with remote controls
Category
Consumer Product
Distribution
Distributed nationwide
SevereCPSC·25280·2025-05-15
Digital Wall Clocks recalled for ingestion hazard from coin battery
Leon Rading Co. Ltd. is recalling digital wall clocks (model PH-05) sold on Amazon because the remote control contains a lithium coin battery that children can easily access and swallow, risking serious internal injury or death.
Product
Digital Wall Clocks
Category
Consumer Product
Distribution
Distributed nationwide
SevereCPSC·25278·2025-05-15
Boyro Baby Convertible High Chairs Recalled for Fall and Entrapment Hazards
Boyro Baby Convertible High Chairs sold on Amazon.com pose a risk of serious injury or death from falls and entrapment. The restraint system is not properly attached and can fail, and the opening between seat and tray is large enough for a child to become trapped.
Product
Boyro Baby Convertible High Chairs
Category
Consumer Product
Distribution
Distributed nationwide
SevereCPSC·25282·2025-05-15
LivingCaring Adult Portable Bed Rails recalled for entrapment and asphyxiation risk
LivingCaring Adult Portable Bed Rails pose a serious risk of entrapment and asphyxiation due to violations of federal safety regulations. About 280 units sold online May 2024–March 2025 are affected; consumers should stop using them immediately.
Product
LivingCaring Adult Portable Bed Rails
Category
Consumer Product
Distribution
Distributed nationwide
SevereCPSC·25281·2025-05-15
PlayTab Rollers Tile Toys Recalled for Magnet Ingestion Hazard
Fat Brain Toy Co. is recalling PlayTab Rollers Tile Toys because they contain magnets that can become loose and be swallowed by children, posing a risk of serious injury or death.
Product
PlayTab Rollers Tile Toys
Category
Consumer Product
Distribution
Distributed nationwide
SevereNHTSA·25V269000·2025-05-15
Volkswagen ID. Buzz third-row bench seats three but has two belts
Volkswagen is recalling certain 2025 ID. Buzz vehicles because the third-row bench is wide enough for three passengers but is designed for two and has only two seat belts, failing FMVSS 208.
Product
VOLKSWAGEN — VOLKSWAGEN ID. BUZZ
Category
Vehicle
Distribution
Distributed nationwide
SevereNHTSA·25V323000·2025-05-15
School bus parking brake can release while wheelchair lift is deployed
International is recalling certain 2025-2026 IC Bus CESB school buses because the parking brake can be released while the wheelchair platform lift is deployed, failing FMVSS 403.
Product
IC BUS — IC BUS CESB
Category
Vehicle
Distribution
Distributed nationwide
HighNHTSA·25V322000·2025-05-15
Toyota Tundra reverse lights can fail from moisture in the assembly
Toyota is recalling certain 2022-2025 Tundra and Tundra Hybrid vehicles because moisture may enter the reverse light assemblies and cause the lights to fail.
Product
TOYOTA — TOYOTA TUNDRA HYBRID, TUNDRA
Category
Vehicle
Distribution
Distributed nationwide
HighCPSC·25283·2025-05-15
Off-Road Motorcycles Recalled Due to Brake Caliper Crack Hazard
KTM is recalling about 19,310 GASGAS and Husqvarna off-road motorcycles from model years 2022–2025 because the front brake caliper can crack, reducing braking effectiveness and creating a crash risk. No injuries have been reported.
Product
GASGAS and Husqvarna Off-Road Motorcycles
Category
Vehicle
Distribution
Distributed nationwide
HighCPSC·25284·2025-05-15
Polaris Ranger XP 1000 NorthStar Recreational Off-Road Vehicles Seat Belt Fastener Recall
Polaris is recalling about 640 Model Year 2023–2025 Ranger XP 1000 NorthStar and NorthStar Crew off-road vehicles because seat belt anchor fasteners may not be properly tightened, risking seat belt separation in a crash and potential ejection of riders.
Product
Model Year 2023-2025 Ranger XP 1000 NorthStar and Ranger XP 1000 NorthStar Crew Recreational Off-Road Vehicles (ROVs)
Category
Vehicle
Distribution
Distributed nationwide
HighCPSC·25287·2025-05-15
Children's Mini Danica Loungewear Sets Recalled for Burn Hazard Risk
BuddyLove is recalling about 940 children's Mini Danica loungewear sets (sizes 3–12) sold from October 2023 through July 2024 because they violate federal flammability standards for children's sleepwear, posing a burn hazard and risk of serious injury or death.
Product
Children's Mini Danica Loungewear Sets
Category
Consumer Product
Distribution
Distributed nationwide