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 2774127760 of 27,884 recalls

Medical DeviceDecember 9, 2010· Alphatec Spine, Inc.

Recalled Item: TI Standard Polyaxial Screw Assembly 6.5MM x 55MM. Part # Recalled by...

The Issue: The recall was initiated because Alphatec Spine confirmed that the TI...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 1, 2010· Siemens Healthcare Diagnostics, Inc.

Recalled Item: BCS(R) Behring Coagulation System Recalled by Siemens Healthcare...

The Issue: Firm has confirmed that if the Cleaner SCS vial becomes empty after...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 1, 2010· Canon Inc.

Recalled Item: Canon Solid State X-ray Imager (Flat Panel/Digital Imager) Recalled by Canon...

The Issue: Screws holding the 55REF circuit board are loosening and roaming inside of...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 12, 2010· Medtronic Navigation, Inc.

Recalled Item: Medtronic 0-arm Imaging System with Software Version 3.1.1 Recalled by...

The Issue: Software Version 3.1.1 does not meet navigational accuracy.

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 10, 2010· Zimmer, Inc.

Recalled Item: 00780302601 MIS 12/14 Slotted Femoral Head Provisional -3.5X26 00780302602...

The Issue: Surgical technique instructions for the Versys and Slotted Provisional...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 10, 2010· Zimmer, Inc.

Recalled Item: 00780302801 MIS 12/14 Slotted Femoral Head Provisional -3.5X28 00780302802...

The Issue: Surgical technique instructions for the Versys and Slotted Provisional...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 10, 2010· Zimmer, Inc.

Recalled Item: . 00789502801 VerSys Femoral Head Provisional 28mm -3.5 00789502802 VerSys...

The Issue: Surgical technique instructions for the Versys and Slotted Provisional...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 10, 2010· Zimmer, Inc.

Recalled Item: 00780302201 MIS 12/14 Slotted Femoral Head Provisional -2X22 00780302202 MIS...

The Issue: Surgical technique instructions for the Versys and Slotted Provisional...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 10, 2010· Zimmer, Inc.

Recalled Item: 00789502601 VerSys Femoral Head Provisional 26mm -3.5 00789502602 VerSys...

The Issue: Surgical technique instructions for the Versys and Slotted Provisional...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 10, 2010· Zimmer, Inc.

Recalled Item: 00780303201 MIS 12/14 Slotted Femoral Head Provisional -3.5X32 00780303202...

The Issue: Surgical technique instructions for the Versys and Slotted Provisional...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 10, 2010· Zimmer, Inc.

Recalled Item: Product 100789502202 VerSys Femoral Head Provisional 22mm +0 00789502203...

The Issue: Surgical technique instructions for the Versys and Slotted Provisional...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 10, 2010· Zimmer, Inc.

Recalled Item: . 00789503601 VerSys Femoral Head Provisional 36mm -3.5 00789503602 VerSys...

The Issue: Surgical technique instructions for the Versys and Slotted Provisional...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 10, 2010· Zimmer, Inc.

Recalled Item: 00780304001 MIS 12/14 Slotted Femoral Head Provisional -3.5X36 00780304002...

The Issue: Surgical technique instructions for the Versys and Slotted Provisional...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 10, 2010· Zimmer, Inc.

Recalled Item: 00789503201 VerSys Femoral Head Provisional 32mm -3.5 00789503202 VerSys...

The Issue: Surgical technique instructions for the Versys and Slotted Provisional...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 10, 2010· Zimmer, Inc.

Recalled Item: 00780303601 MIS 12/14 Slotted Femoral Head Provisional -3.5X36 00780303602...

The Issue: Surgical technique instructions for the Versys and Slotted Provisional...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 10, 2010· Zimmer, Inc.

Recalled Item: 00789504001 VerSys Femoral Head Provisional 40mm -3.5 00789504002 VerSys...

The Issue: Surgical technique instructions for the Versys and Slotted Provisional...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 5, 2010· Sunquest Information Systems, Inc.

Recalled Item: Sunquest Laboratory LabAccess Results Workstation (LARS) Recalled by...

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 DeviceSeptember 27, 2010· Medtronic Xomed, Inc.

Recalled Item: Interfaces subject to recall: Medtronic NIM (Nerve Integrity Monitor) 3.0...

The Issue: In January 2010, Medtronic issued a recall of Medtronic NIM 3.0 Patient...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 27, 2010· Medtronic Xomed, Inc.

Recalled Item: Interfaces subject to recall: Medtronic NIM (Nerve Integrity Monitor) 3.0...

The Issue: In January 2010, Medtronic issued a recall of Medtronic NIM 3.0 Patient...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 27, 2010· Medtronic Xomed, Inc.

Recalled Item: Interfaces subject to recall: Medtronic NIM (Nerve Integrity Monitor) 3.0...

The Issue: In January 2010, Medtronic issued a recall of Medtronic NIM 3.0 Patient...

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

Class II — Potential Health HazardOngoing