Product Recalls in West Virginia

Product recalls affecting West Virginia — including food, drugs, consumer products, medical devices, and vehicles distributed to West Virginia. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 2,393 recalls have been distributed to West Virginia in the last 12 months.

48,376 total recalls
2,393 in last 12 months

Showing 2234122360 of 27,884 recalls

Medical DeviceMarch 6, 2015· Wright Medical Technology, Inc.

Recalled Item: CROSSCHECK(R) Plating system Recalled by Wright Medical Technology, Inc. Due...

The Issue: The minor diameter, major diameter, thread pitch, and pitch on the...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceMarch 6, 2015· Wright Medical Technology, Inc.

Recalled Item: CROSSCHECK(R) Plating system Recalled by Wright Medical Technology, Inc. Due...

The Issue: The minor diameter, major diameter, thread pitch, and pitch on the...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceMarch 6, 2015· Wright Medical Technology, Inc.

Recalled Item: CROSSCHECK(R) Plating system Recalled by Wright Medical Technology, Inc. Due...

The Issue: The minor diameter, major diameter, thread pitch, and pitch on the...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceMarch 6, 2015· Wright Medical Technology, Inc.

Recalled Item: CROSSCHECK(R) Plating system Recalled by Wright Medical Technology, Inc. Due...

The Issue: The minor diameter, major diameter, thread pitch, and pitch on the...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceMarch 6, 2015· Wright Medical Technology, Inc.

Recalled Item: CROSSCHECK(R) Plating system Recalled by Wright Medical Technology, Inc. Due...

The Issue: The minor diameter, major diameter, thread pitch, and pitch on the...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceMarch 6, 2015· Wright Medical Technology, Inc.

Recalled Item: CROSSCHECK(R) Plating system Recalled by Wright Medical Technology, Inc. Due...

The Issue: The minor diameter, major diameter, thread pitch, and pitch on the...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceMarch 6, 2015· Wright Medical Technology, Inc.

Recalled Item: CROSSCHECK(R) Plating system Recalled by Wright Medical Technology, Inc. Due...

The Issue: The minor diameter, major diameter, thread pitch, and pitch on the...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceMarch 6, 2015· Wright Medical Technology, Inc.

Recalled Item: CROSSCHECK(R) Plating system Recalled by Wright Medical Technology, Inc. Due...

The Issue: The minor diameter, major diameter, thread pitch, and pitch on the...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceMarch 5, 2015· Maquet Cardiovascular Us Sales, Llc

Recalled Item: HLS/HIT Set Advanced with Bioline and/or Softline Coating Console Product...

The Issue: A potential issue was detected that could result in blood leakage from the...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceMarch 5, 2015· Merge Healthcare, Inc.

Recalled Item: Merge LIS software. Recalled by Merge Healthcare, Inc. Due to There is a...

The Issue: There is a potential for duplicate container numbers to be created for patients.

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceMarch 5, 2015· Maquet Cardiovascular Us Sales, Llc

Recalled Item: Quadrox-iD Adult Diffusion Membrane Oxygenator Product Usage: The Quadrox-iD...

The Issue: A potential issue was detected that could result in blood leakage from the...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceMarch 5, 2015· SpineFrontier, Inc.

Recalled Item: SpineFrontier MISquito Percutaneous Pedicle Screw System Surgical Technique...

The Issue: The PedFuse Pedicle Screw Rod Caliper included with the MISquito Pedicle...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceMarch 5, 2015· Codman & Shurtleff, Inc.

Recalled Item: CODMAN 3000 Series Set- Huber needles. Used in combination Recalled by...

The Issue: Needle is leaking from hub/needle cannula connection

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceMarch 5, 2015· GE Healthcare

Recalled Item: GE Healthcare Millennium VG Recalled by GE Healthcare Due to GE Healthcare...

The Issue: GE Healthcare has recently become aware of a potential safety issue due to a...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceMarch 4, 2015· Cardiovascular Systems, Inc.

Recalled Item: Diamondback 360 Coronary Orbital Atherectomy System Recalled by...

The Issue: The OAD saline sheath outer layer may flake off from the catheter due to...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class I — Serious Health HazardOngoing
Medical DeviceMarch 4, 2015· Ossur H / F

Recalled Item: LP Rotate Foot System prosthetic device for fitting lower extremity Recalled...

The Issue: The threads of the outer tube of the shock module of LP Rotate are too...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceMarch 4, 2015· RAYSEARCH LABORATORIES AB

Recalled Item: RayStation Radiation Therapy Treatment Planning System Recalled by RAYSEARCH...

The Issue: An issue with photon dose calculation for DMLC (Dynamic MLC) plans for...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceMarch 4, 2015· DePuy Orthopaedics, Inc.

Recalled Item: LCS COMPLETE RPS inserts Recalled by DePuy Orthopaedics, Inc. Due to The LCS...

The Issue: The LCS COMPLETE RPS Knee System has higher rates of revision in Australia...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceMarch 4, 2015· DePuy Orthopaedics, Inc.

Recalled Item: LCS COMPLETE RPS Femoral Implants Recalled by DePuy Orthopaedics, Inc. Due...

The Issue: The LCS COMPLETE RPS Knee System has higher rates of revision in Australia...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceMarch 3, 2015· Intuitive Surgical, Inc.

Recalled Item: da Vinci Xi Surgical System Recalled by Intuitive Surgical, Inc. Due to...

The Issue: Correction due to a fault that causes distal SUJ (DSUJ) failures that...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing