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. 2,437 recalls have been distributed to West Virginia in the last 12 months.

48,376 total recalls
2,437 in last 12 months

Showing 1938119400 of 27,884 recalls

Medical DeviceJuly 15, 2016· Roche Diagnostics Operations, Inc.

Recalled Item: cobas p 612 Pre-Analytical Instrument calculator/data processing module...

The Issue: Roche has received four reports of injury caused by the sharp edge of the...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 15, 2016· Roche Diagnostics Operations, Inc.

Recalled Item: RSD 800A Aliquoting System calculator/data processing module Recalled by...

The Issue: Roche has received four reports of injury caused by the sharp edge of the...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 15, 2016· Roche Diagnostics Operations, Inc.

Recalled Item: cobas 6000 Series system c6000 Recalled by Roche Diagnostics Operations,...

The Issue: Roche has received four reports of injury caused by the sharp edge of the...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 15, 2016· Roche Diagnostics Operations, Inc.

Recalled Item: Roche COBAS INTEGRA 800 /800 CTS Analyzer Analyzer Recalled by Roche...

The Issue: Roche has received four reports of injury caused by the sharp edge of the...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 15, 2016· Roche Diagnostics Operations, Inc.

Recalled Item: Modular Pre Analytics ( EVO/Plus) Product Usage: The RSD 800A Recalled by...

The Issue: Roche has received four reports of injury caused by the sharp edge of the...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 15, 2016· Roche Diagnostics Operations, Inc.

Recalled Item: cobas 8000 Modular Analyzer Series c8000 Recalled by Roche Diagnostics...

The Issue: Roche has received four reports of injury caused by the sharp edge of the...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 15, 2016· Roche Diagnostics Operations, Inc.

Recalled Item: cobas p 312 Pre-Analytical System calculator/data processing module Recalled...

The Issue: Roche has received four reports of injury caused by the sharp edge of the...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 15, 2016· Roche Diagnostics Operations, Inc.

Recalled Item: cobas 6800/8800 system Hepatitis Viral B DNA Detection Product Usage:...

The Issue: Roche has received four reports of injury caused by the sharp edge of the...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 15, 2016· Elekta, Inc.

Recalled Item: MOSAIQ Oncology Information System Recalled by Elekta, Inc. Due to It is...

The Issue: It is possible that a change to an Order Set will not be saved in the...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 15, 2016· Topcon Medical Laser Systems, Inc

Recalled Item: Opthalmic: PASCAL Synthesis is an ophthalmic scanning laser system. The...

The Issue: Topcon discovered an anomaly with titration, only when EpM is turned on...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 14, 2016· ORTHO-CLINICAL DIAGNOSTICS

Recalled Item: VITROS Immunodiagnostic Products Estradiol Reagent Pack Recalled by...

The Issue: Ortho Clinical Diagnostics has issued a recall of their VITROS...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 14, 2016· Intuitive Surgical, Inc.

Recalled Item: CURVED-TIP STAPLER 30 Recalled by Intuitive Surgical, Inc. Due to Field...

The Issue: Field failures were reported related to the da Vinci Xi Surgical System...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 14, 2016· Straumann Manufacturing, Inc.

Recalled Item: Straumann Bone Level Implant Recalled by Straumann Manufacturing, Inc. Due...

The Issue: Misalignment with the Loxim transfer piece markings, the positioning of the...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 14, 2016· Merge Healthcare, Inc.

Recalled Item: Merge RadSuite Recalled by Merge Healthcare, Inc. Due to It was reported by...

The Issue: It was reported by a customer that RadSuite images are not appearing as...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 14, 2016· Straumann Manufacturing, Inc.

Recalled Item: Straumann Bone Level Implant Recalled by Straumann Manufacturing, Inc. Due...

The Issue: Misalignment with the Loxim transfer piece markings, the positioning of the...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 14, 2016· Intuitive Surgical, Inc.

Recalled Item: STAPLER Recalled by Intuitive Surgical, Inc. Due to Field failures were...

The Issue: Field failures were reported related to the da Vinci Xi Surgical System...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 14, 2016· Intuitive Surgical, Inc.

Recalled Item: STAPLER 30 Recalled by Intuitive Surgical, Inc. Due to Field failures were...

The Issue: Field failures were reported related to the da Vinci Xi Surgical System...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 13, 2016· Siemens Medical Solutions USA, Inc

Recalled Item: ARTIS ZEE AND ZEEGO Recalled by Siemens Medical Solutions USA, Inc Due to...

The Issue: The possibility exists for contaminants, in the form of biomass, to develop...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 13, 2016· Siemens Medical Solutions USA, Inc

Recalled Item: AXIOM ARTIS MODULAR ANGIOGRAPHY SYSTEM Recalled by Siemens Medical Solutions...

The Issue: The possibility exists for contaminants, in the form of biomass, to develop...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 13, 2016· Diasorin Inc.

Recalled Item: LIAISON Estradiol II Gen Recalled by Diasorin Inc. Due to DiaSorin is...

The Issue: DiaSorin is issuing an urgent medical device correction for the LIAISON¿...

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

Class II — Potential Health HazardOngoing