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 2496124980 of 27,884 recalls

Medical DeviceSeptember 19, 2013· GE Healthcare, LLC

Recalled Item: Multi Absorber Original Recalled by GE Healthcare, LLC Due to GE Healthcare...

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

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

Class I — Serious Health HazardOngoing
Medical DeviceSeptember 19, 2013· AGFA Corp.

Recalled Item: IMPAX 5.2 DB Server (running Oracle 10.1.0.4.0) Recalled by AGFA Corp. Due...

The Issue: System downtime and/or slow performance may result if software in use is an...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 18, 2013· GE Healthcare Beijing , Hangwei Medical Systems, Co. LTD

Recalled Item: GE Brivo OEC715/785/865 C-Arm Recalled by GE Healthcare Beijing , Hangwei...

The Issue: GE is recalling certain lots of GE Brivo OEC715/785/865 C-Arm due to the...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 18, 2013· Advanced Sterilization Products

Recalled Item: STERRAD 100NX Cassettes The STERRAD Sterilization System is a low Recalled...

The Issue: Advanced Sterilization Products (ASP) is recalling the three lots (13F049,...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 18, 2013· Advanced Sterilization Products

Recalled Item: STERRAD 200 Sterilizer (Single Door) Recalled by Advanced Sterilization...

The Issue: Advanced Sterilization Products (ASP) is recalling the STERRAD 200...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 18, 2013· Richard Wolf Medical Instruments Corp.

Recalled Item: Individual units labeled in part: Recalled by Richard Wolf Medical...

The Issue: Richard Wolf Medical Instrument Corporation recieved a complaint stating...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 17, 2013· DeRoyal Industries Inc

Recalled Item: DeRoyal (R) Aquarius Hot/Cold Therapy Combo Unit Recalled by DeRoyal...

The Issue: The unit displays an error code of hose kinking when no hose kink is...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 17, 2013· DeRoyal Industries Inc

Recalled Item: DeRoyal (R) Aquarius Hot/Cold Therapy Combo Unit Recalled by DeRoyal...

The Issue: The unit displays an error code of hose kinking when no hose kink is...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 17, 2013· DeRoyal Industries Inc

Recalled Item: DeRoyal (R) Aquarius Hot/Cold Therapy Combo Unit Recalled by DeRoyal...

The Issue: The unit displays an error code of hose kinking when no hose kink is...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 17, 2013· DeRoyal Industries Inc

Recalled Item: DeRoyal (R) Aquarius Hot/Cold Therapy Combo Unit Recalled by DeRoyal...

The Issue: The unit displays an error code of hose kinking when no hose kink is...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 17, 2013· Siemens Healthcare Diagnostics, Inc.

Recalled Item: Siemens Dimension LOCI TNI Troponin I Calibrator RC 621. The Recalled by...

The Issue: Siemens Dimension LOCI TNI Troponin I calibrator lot 3DD007 may demonstrate...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 17, 2013· DeRoyal Industries Inc

Recalled Item: Aquarius (TM) TEMPERATURE THERAPY Recalled by DeRoyal Industries Inc Due to...

The Issue: The unit displays an error code of hose kinking when no hose kink is...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 17, 2013· DeRoyal Industries Inc

Recalled Item: DeRoyal (R) Aquarius Hot/Cold Therapy Combo Unit Recalled by DeRoyal...

The Issue: The unit displays an error code of hose kinking when no hose kink is...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 16, 2013· Abbott Medical Optics, Inc.

Recalled Item: STAR Excimer Laser System Recalled by Abbott Medical Optics, Inc. Due to...

The Issue: This corrective action will address an identified failure of the lamp and...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 16, 2013· GE Healthcare, LLC

Recalled Item: GE Healthcare Recalled by GE Healthcare, LLC Due to GE Healthcare has...

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

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

Class I — Serious Health HazardOngoing
Medical DeviceSeptember 16, 2013· Sekisui Diagnostics LLC

Recalled Item: Product Name: OSOM C. Difficile Toxin A/B Test Catalog Numbers: Recalled by...

The Issue: Sekisuki Diagnostics has issued a Product Correction for certain lot numbers...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 16, 2013· Roche Diagnostics Operations, Inc.

Recalled Item: COBAS INTEGRA 800 Analyzer with software 9864.C2 Cobas. COBAS Part Recalled...

The Issue: Roche COBAS INTEGRA 800 system, Software Version 9864.C2 does not perform...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 16, 2013· Abbott Medical Optics, Inc.

Recalled Item: STAR Excimer Laser System Recalled by Abbott Medical Optics, Inc. Due to...

The Issue: This corrective action will address an identified failure of the lamp and...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 16, 2013· Abbott Medical Optics, Inc.

Recalled Item: STAR ActiveTrak Excimer Laser System Recalled by Abbott Medical Optics, Inc....

The Issue: This corrective action will address an identified failure of the lamp and...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 16, 2013· Abbott Medical Optics, Inc.

Recalled Item: STAR Excimer Laser System with Variable Spot Scanning Recalled by Abbott...

The Issue: This corrective action will address an identified failure of the lamp and...

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

Class II — Potential Health HazardOngoing