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. 2,356 recalls have been distributed to West Virginia in the last 12 months.

48,376 total recalls
2,356 in last 12 months

Showing 2758127600 of 27,884 recalls

Medical DeviceDecember 19, 2011· Advanced Neuromodulation Systems Inc.

Recalled Item: Eon Mini Neurostimulation (IPG) System (Model 3788) Recalled by Advanced...

The Issue: The firm has received 112 complaints of the Eon Mini IPGs that lost the...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 19, 2011· Advanced Neuromodulation Systems Inc.

Recalled Item: Eon (Model 3716) IPG is a dual channel Recalled by Advanced Neuromodulation...

The Issue: As of 11/30/2011, St. Jude Medical has received 110 patient complaints of...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 15, 2011· Beckman Coulter Inc.

Recalled Item: Synchron Systems Synchron Calibrator Multi Calibrator Diskettes Recalled by...

The Issue: The recall was initiated because Beckman Coulter has confirmed a mislabeling...

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

Class III — Low RiskOngoing
Medical DeviceDecember 13, 2011· Beckman Coulter Inc.

Recalled Item: UniCel DxH Slidemaker Stainer Instrument System Recalled by Beckman Coulter...

The Issue: The recall was initiated because Beckman Coulter has confirmed that the DxH...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 13, 2011· Beckman Coulter Inc.

Recalled Item: UniCel DxH Slidemaker Stainer Stainer Floor Cabinet Recalled by Beckman...

The Issue: The recall was initiated because Beckman Coulter has confirmed that the DxH...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 12, 2011· Ormco/Sybronendo

Recalled Item: Vector TAS Modular Driver Recalled by Ormco/Sybronendo Due to The...

The Issue: The Instructions For Use (IFUs) for Vector TAS Modular Driver for some...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 9, 2011· Progressive Medical Inc

Recalled Item: Progressive Medical PMI Endoscopic Dissector with Kittner Tip (5mm x 40cm)...

The Issue: Some of the sterile packages had broken seals.

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 8, 2011· Tripath Imaging, Inc.

Recalled Item: PrepStain Upgrade Kit: 1.3.0.3/1.2 DiTi Cone. The PrepStain System is...

The Issue: Some Prep Stain Kit, 1.2 DiTi Cones have been found to be leaking and the...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 8, 2011· Tripath Imaging, Inc.

Recalled Item: PrepStain Slide Processor. The PrepStain System is a liquid-based thin...

The Issue: Some Prep Stain Kit, 1.2 DiTi Cones have been found to be leaking and the...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 8, 2011· Tripath Imaging, Inc.

Recalled Item: PrepStain PM Kit Recalled by Tripath Imaging, Inc. Due to Some Prep Stain...

The Issue: Some Prep Stain Kit, 1.2 DiTi Cones have been found to be leaking and the...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 8, 2011· Tripath Imaging, Inc.

Recalled Item: PrepStain Kit: 1.2 DiTi Cone. The PrepStain System is a Recalled by Tripath...

The Issue: Some Prep Stain Kit, 1.2 DiTi Cones have been found to be leaking and the...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 5, 2011· Sunquest Information Systems, Inc.

Recalled Item: Sunquest Laboratory Versions 6.4 and later using Microbiology Result Entry...

The Issue: The recall was initiated because Sunquest has confirmed that the Sunquest...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 30, 2011· Toshiba American Medical Systems Inc

Recalled Item: TSX-IOI: AQUILION 32/64 Recalled by Toshiba American Medical Systems Inc Due...

The Issue: The firm initiated this recall due to a potential software issue. The DLP...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 30, 2011· Abbott Vascular

Recalled Item: Brand Name: RX Accunet Embolic Protection System Common Name: RX Recalled by...

The Issue: The recall was initiated because Abbot Vascular has discovered that the...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 21, 2011· GE Healthcare, LLC

Recalled Item: SIGNA INFINITY MR SYSTEM WITH EXCITE TECHNOLOGY GE 3.0T SIGNA Recalled by GE...

The Issue: Screen save images are included in wrong exam due to duplicate UID creation....

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 17, 2011· Kerr Corporation

Recalled Item: Freedom Cordless LED Light System. Freedom System Recalled by Kerr...

The Issue: The firm recalled the Freedom Cordless LED Headlight because some units were...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 15, 2011· Sunquest Information Systems, Inc.

Recalled Item: Sunquest Laboratory : intended for use by professionals working in Recalled...

The Issue: Online calculations may not be performed as expected or may yield results...

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

Class III — Low RiskOngoing
Medical DeviceNovember 14, 2011· US Endoscopy Group Inc

Recalled Item: Endoscopic retrieval device. The disposable Raptor grasping device in...

The Issue: When the outer catheter is either coiled or in a contorted configuration...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 4, 2011· Biomet 3i, LLC

Recalled Item: Implant Recalled by Biomet 3i, LLC Due to On November 3, 2011 Biomet 3i,...

The Issue: On November 3, 2011 Biomet 3i, Palm Beach Gardens, FL initiated a recall of...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 3, 2011· Sunquest Information Systems, Inc.

Recalled Item: Sunquest Laboratory Recalled by Sunquest Information Systems, Inc. Due to...

The Issue: Sunquest is recalling Sunquest Laboratory version 7.0 because when saving an...

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

Class II — Potential Health HazardOngoing