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Recalls in West Virginia

Recalls sold in West Virginia, including nationwide recalls, newest first.
Agency
Risk level
Date
Sold in

14 recalls

Stryker Neurovascular Inzone Detachment System

The INZONE DETACHMENT SYSTEM may experience premature battery drain, causing it to not power on or be unable to detach a coil.

Moderate risk, FDA, Device defect

Airstream Classic (2026) and Airstream Interstate (2025-2027)

The printed circuit board in certain Airstream trailers and vehicles may overheat, increasing the risk of a fire.

NHTSA, Electrical system defect

Hyundai Tucson, Hyundai Tucson Hybrid, and Hyundai Tucson Plug-In Hybrid (2025-2026)

The instrument panel display in certain Hyundai Tucson vehicles may fail, increasing the risk of a crash.

NHTSA, Electrical system defect

Ford Bronco

Fender flares on certain Ford Broncos may detach, becoming a road hazard and increasing crash risk.

NHTSA, Vehicle structure defect

Ford Expedition (2018-2021), Ford Explorer (2020-2021), Ford F-150 (2021), and 2 more

The transmission park pawl may engage while the vehicle is in motion, causing park system damage and a rollaway risk.

NHTSA, Transmission or drivetrain defect

Harbinger Motors Step Van and Stripped Chassis

The steering gear mounting bolts may come loose or break, causing loss of steering control and increasing crash risk.

NHTSA, Steering defect

Elgin Pelican (2024-2026)

Elgin Pelican vehicles have high voltage batteries that may fail and overheat, increasing the risk of a fire.

NHTSA, Electrical system defect

Abbott Determine HIV 1/2 Ag/Ab Combo

Abbott Diagnostics has noticed a negative trend in false positive complaints for Determine" HIV 1/2 Ag/Ab Combo 25T kits (Catalog 7D2648).

Moderate risk, FDA

6 recalls

Direct Rx Duloxetine and Cymbalta Capsules

Duloxetine D/R contains an impurity above the FDA recommended interim limit.

Moderate risk, FDA, Drug impurity

Amgen Corlanor and Sensipar Tablets

Corlanor (ivabradine) tablets contain a foreign substance, and Sensipar (cinacalcet) Tablets have CGMP deviations.

Moderate risk, FDA, Foreign object

Zimmer Off-Axis Comprehensive Shoulder System Reamer Guides

Five complaints have been received identifying issues where the plastic guides were catching during reaming, leading to breakage.

Moderate risk, FDA, Device defect

Chevrolet Express and GMC Savana Vehicles

The steering gear assembly may have a nut that was not properly tightened, which can cause loss of steering control and increase crash risk.

NHTSA, Steering defect

Rockford Fosgate Amplifier Kits

The amplifier kits have inadequate fuse protection that can increase the risk of a fire.

NHTSA, Electrical system defect

Ricon S-Series and K-Series Wheelchair Lifts

Wheelchair lifts may fail to stop, increasing injury risk.

NHTSA, Mobility equipment defect

6 recalls

Major Methylergonovine Maleate Tablets

Methylergonovine Maleate Tablets are subpotent.

Moderate risk, FDA, Wrong drug strength

Midwest Legacy Raw Beef Dog Food BLT & Bones

Midwest Legacy Raw Beef Dog Food BLT & Bones may be contaminated with Salmonella, Listeria, and E. coli O157:H7.

High risk, FDA, Salmonella

Ajanta Pharma Fenofibrate Capsules

Fenofibrate Capsules, USP 200 mg, have CGMP deviations.

Moderate risk, FDA, Manufacturing problem

Philips Avalon Fetal Monitor

The Philips Avalon Fetal Monitor has incorrect speaker connector assembly that can cause loss of speaker output.

Moderate risk, FDA, Device defect

Intuitive Surgical Da Vinci PSS SP1098

The Da Vinci Assy, PSS, SP1098 may have a retainer pin issue that can cause uncontrolled motion.

Moderate risk, FDA, Device defect

Forest River 2025-2026 NOBO, Ibex, and 2025-2027 RPOD Recreational Trailers

Recreational trailers have mislabeled 110V circuits that can cause electrical shock.

NHTSA, Electrical system defect

2 recalls

Airxcel MaxxAir N-Series Maxxfan Rooftop Ventilation Fans

MaxxAir N-Series Maxxfan rooftop ventilation fans have a printed circuit board that may overheat, posing a fire risk.

NHTSA, Vehicle equipment defect

Indian Motorcycle Company 2026 Chief Vintage Motorcycles

The 2026 Chief Vintage motorcycles have an incorrect rear rim width on the VIN label, which could lead to loss of control and a crash.

NHTSA, Vehicle equipment defect

17 recalls

Arizer Solo III Portable Electronic Vaporizers

Arizer Solo III portable vaporizers can explode or ignite, posing fire and burn hazards.

CPSC, Fire hazard

BABESIDE Doll and Stroller Toys

BABESIDE doll and stroller toys have small parts that can choke young children, posing a risk of serious injury or death.

CPSC, Choking hazard

GOPO TOYS Pull String Teething Toys

Pull string teething toys have silicone strings that are too small and long, posing a choking hazard.

CPSC, Choking hazard

Joolz Aer2 Car Seat Adapters for Joolz Aer 2 Stroller

The Joolz Aer2 Car Seat Adapters can fail to attach properly, allowing the car seat to fall and posing a risk of serious injury.

CPSC, Fall hazard

CooCooBaby Baby Loungers

CooCooBaby Baby Loungers have unsafe sides and padding, posing suffocation and fall hazards.

CPSC, Suffocation hazard

Michley Children's Pajamas

Michley children's pajamas violate flammability standards, posing a risk of serious burn injuries or death.

CPSC, Burn hazard

Veseacky Pajama Sets

Veseacky Pajama Sets violate children's sleepwear safety standards, posing a burn hazard that can cause serious injury or death.

CPSC, Burn hazard

Keystone Topical Anesthetic Gels

Topical anesthetic gels may have defective containers with incomplete seals.

Moderate risk, FDA, Packaging defect

STAAR ICL Calculation Software

The STAAR ICL Calculation Software has a coding issue that affects the implant orientation diagram printout.

Moderate risk, FDA, Software defect

Inspire Respiratory Sensing and Stimulation Lead

The Inspire Respiratory Sensing Lead has an incorrect Use By Date, which may lead to unplanned revision surgery.

Moderate risk, FDA, Labeling error

BD Connecta Stopcocks

BD Connecta BD Luer-Lok 360 Stopcocks may have an unstable connection at Port C when used with a plastic luer-lok syringe.

Moderate risk, FDA, Device defect

Merit Medical Systems Splashwire Hydrophilic Guide Wire

The Splashwire Hydrophilic Guide Wire has unsealed portions of pouches.

Moderate risk, FDA, Packaging defect

Piaggio 2026 Liberty 50 and Liberty 150 motorcycles

The 2026 Liberty 50 and Liberty 150 motorcycles have a headlight that may fail, reducing visibility and increasing crash risk.

NHTSA, Electrical system defect

2026 Toyota BZ, Lexus RZ, and Subaru Solterra Battery Electric Vehicles

The electronic control unit may experience a fault, resulting in a loss of drive power.

NHTSA, Electrical system defect

Farber Specialty 2025 45 MCXCR and 2025-2026 HX620 SBA 6X4 Emergency Vehicles

The touchscreen display may fail, preventing activation of emergency lights and equipment, increasing crash and injury risk.

NHTSA, Vehicle equipment defect

Cadillac Vistiq

The third-row power seatback may fail to reverse when activated, and a person may be trapped, increasing injury risk.

NHTSA, Seat defect

Beta Bionics iLet Bionic Pancreas

This can lead to hyperglycemia.

Moderate risk, FDA, Software defect

6 recalls

Endo Buprenorphine HCl Injection

Buprenorphine HCl injection has crystallization identified as Buprenorphine free base.

Moderate risk, FDA, Quality problem

Howmedica Osteonics Tri TS Baseplate

Stryker has identified that Triathlon Universal Baseplate Size 3 (lot UZD9IB), is contained in packaging labeled as Triathlon Universal Baseplate Size 4 (lot TYX7OB), and Triathlon Universal Baseplate Size 4 (lot TYX7OB), is contained in packaging labeled as Triathlon Universal Baseplate Size 3, (lot UZD9IB).

Moderate risk, FDA, Labeling error

Medline Urethral Catheters and Procedure Kits

Medline urethral catheters and kits may have surface irregularities or connector issues.

Moderate risk, FDA, Quality testing problem

GE HealthCare Giraffe OmniBed Devices

The Giraffe OmniBed has a potential issue with the canopy soffit that could cause patient injury.

Moderate risk, FDA, Device defect

ConMed AirSeal Access Ports and Obturators

ConMed AirSeal Access Port and Obturator may cause overpressure alerts.

Moderate risk, FDA, Device defect

Mito Red Light Super Mobile

The near-infrared therapy device contains a lithium-ion battery that may malfunction, causing it to catch fire or burst into flames.

Moderate risk, FDA, Device defect

4 recalls

Nutrisystem Chocolate Cheesecake

Nutrisystem Chocolate Cheesecake contains an undeclared allergen, soy.

Moderate risk, FDA, Undeclared soy

DirectCHECK ACT-LR Whole Blood Quality Control, Level 2

The whole blood quality control has labeling with an incorrect performance range.

Moderate risk, FDA, Labeling error

Arrogantf Spa Drain Covers

Spa drain covers pose entrapment and drowning hazards due to violating safety standards.

CPSC, Entrapment hazard

Storyteller Overland GXV Hilt Vehicles

GXV Hilt vehicles have a secondary alternator pulley that may fail, causing loss of power brakes and power steering.

NHTSA, Electrical system defect

6 recalls

Ajanta Pharma Aripiprazole Tablets

Aripiprazole Tablets USP are mislabeled, containing Voriconazole Tablets instead.

Moderate risk, FDA, Labeling error