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. 2,367 recalls have been distributed to West Virginia in the last 12 months.

48,376 total recalls
2,367 in last 12 months

Showing 2546125480 of 27,884 recalls

Medical DeviceJune 12, 2013· Ortho-Clinical Diagnostics

Recalled Item: VITROS Chemistry Products UPRO Slides packaged as 90 slides/pack catalog...

The Issue: Ortho Clinical Diagnostics is recalling Slide Dispense cartridges used with...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 11, 2013· Philips Healthcare Inc.

Recalled Item: Philips Healthcare MobileDiagnostwDR system. Mobile Digital radiography...

The Issue: The Instructions for Use (IFU) for the MobileDiagnost wDR fails to comply...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 11, 2013· Integra LifeSciences Corp.

Recalled Item: Integra Licox Brain Tissue Oxygen Monitoring Recalled by Integra...

The Issue: Integra LifeSciences Corporation has determined that there is a possibility...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 11, 2013· Integra LifeSciences Corp.

Recalled Item: Integra Licox Brain Tissue Oxygen Monitoring 1 x Complete Brain Recalled by...

The Issue: Integra LifeSciences Corporation has determined that there is a possibility...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 11, 2013· Integra LifeSciences Corp.

Recalled Item: Integra Licox Brain Tissue Oxygen Monitoring 1 x Complete Brain Recalled by...

The Issue: Integra LifeSciences Corporation has determined that there is a possibility...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 11, 2013· Integra LifeSciences Corp.

Recalled Item: Integra Licox Brain Tissue Oxygen Monitoring 1 x Dual Lumen Recalled by...

The Issue: Integra LifeSciences Corporation has determined that there is a possibility...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 11, 2013· Integra LifeSciences Corp.

Recalled Item: Integra Licox Brain Tissue Oxygen Monitoring Recalled by Integra...

The Issue: Integra LifeSciences Corporation has determined that there is a possibility...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 11, 2013· Integra LifeSciences Corp.

Recalled Item: Integra Licox Brain Tissue Oxygen Monitoring 1 x Complete Brain Recalled by...

The Issue: Integra LifeSciences Corporation has determined that there is a possibility...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 11, 2013· Integra LifeSciences Corp.

Recalled Item: Inegra Licox Brain Tissue Oxygen Monitoring 1 x Complete Brain Recalled by...

The Issue: Integra LifeSciences Corporation has determined that there is a possibility...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 11, 2013· Integra LifeSciences Corp.

Recalled Item: Integra Licox Brain Tissue Oxygen Monitoring 1 x Dual Lumen Recalled by...

The Issue: Integra LifeSciences Corporation has determined that there is a possibility...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 11, 2013· Zimmer, Inc.

Recalled Item: Bigliani/Flatow¿ The Complete Shoulder Solution Recalled by Zimmer, Inc. Due...

The Issue: The firm is initiating a removal of one lot of the Bigliani/Flatow Humeral...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 11, 2013· Integra LifeSciences Corp.

Recalled Item: Integra Licox Brain Tissue Oxygen Monitoring 1 x Complete Brain Recalled by...

The Issue: Integra LifeSciences Corporation has determined that there is a possibility...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 11, 2013· Synthes USA HQ, Inc.

Recalled Item: Synthes Flexible Medullary Reamer. Intended to be used to facilitate...

The Issue: Due to the coiled design for this product, the product is difficult to clean...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 11, 2013· GE Healthcare It

Recalled Item: The Centricity PACS Workstation is intended for use as a Recalled by GE...

The Issue: GE has recently become aware of potential issues due to out of context...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 11, 2013· Church & Dwight Inc

Recalled Item: Sodium Bicarbonate Recalled by Church & Dwight Inc Due to Church and Dwight...

The Issue: Church and Dwight Co., Inc. has initiated a recall for Sodium Bicarbonate,...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 11, 2013· Integra LifeSciences Corp.

Recalled Item: Integra Licox Brain Tissue Oxygen Monitoring 1 x Complete Brain Recalled by...

The Issue: Integra LifeSciences Corporation has determined that there is a possibility...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 10, 2013· Steritec Products Mfc. Co., Inc.

Recalled Item: EZTest Steam Biological Indicator Recalled by Steritec Products Mfc. Co.,...

The Issue: Mesa Labs, based out of Bozeman, MT, informed SteriTec Products, Inc. of a...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 10, 2013· Steritec Products Mfc. Co., Inc.

Recalled Item: Medline Steam Biological Indicators Recalled by Steritec Products Mfc. Co.,...

The Issue: Mesa Labs, based out of Bozeman, MT, informed SteriTec Products, Inc. of a...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 10, 2013· Steritec Products Mfc. Co., Inc.

Recalled Item: Cardinal Steam Biological Indicator Recalled by Steritec Products Mfc. Co.,...

The Issue: Mesa Labs, based out of Bozeman, MT, informed SteriTec Products, Inc. of a...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 10, 2013· Zimmer, Inc.

Recalled Item: Persona (TM) The Personalized Knee System Tibial Articular Surface...

The Issue: Zimmer had received complaints that reported breakage of the Persona Knee...

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

Class II — Potential Health HazardOngoing