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 2750127520 of 27,884 recalls

Medical DeviceMarch 27, 2012· Nidek Inc

Recalled Item: MC-500 Multicolor Laser Photocoagulator Recalled by Nidek Inc Due to The...

The Issue: The spot size control of the scan delivery unit of the MC-500 Multicolor...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 23, 2012· B. Braun Medical, Inc.

Recalled Item: Space Pump Pole Clamps for the Infusomat Space Pump Recalled by B. Braun...

The Issue: Firm has become aware of the potential for breakage of the pole clamp...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 23, 2012· Colgate Palmolive Company

Recalled Item: Colgate 360 Replaceable Head Battery Powered Bonus Twin Pack Toothbrush...

The Issue: Brush battery cap was forcibly blown off at the end of the brush handle.

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 23, 2012· Colgate Palmolive Company

Recalled Item: Colgate 360 Replaceable Head Battery Powered Toothbrush Medium Dist....

The Issue: Brush battery cap was forcibly blown off at the end of the brush handle.

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 23, 2012· Colgate Palmolive Company

Recalled Item: Colgate Adult Motion Whitening Battery Toothbrush Dist. by Recalled by...

The Issue: Brush battery cap was forcibly blown off at the end of the brush handle.

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 23, 2012· B. Braun Medical, Inc.

Recalled Item: Infusomat(R) Space Pump (US Version) with software version 686G030103...

The Issue: Firm became aware of the potential for breakage of the anti free flow clip...

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

Class I — Serious Health HazardOngoing
Medical DeviceMarch 23, 2012· Colgate Palmolive Company

Recalled Item: Colgate 360 Replaceable Head Battery Powered Toothbrush Soft Recalled by...

The Issue: Brush battery cap was forcibly blown off at the end of the brush handle.

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 23, 2012· Colgate Palmolive Company

Recalled Item: Colgate Adult Motion Battery Toothbrush Dist. by Colgate-Palmolive Recalled...

The Issue: Brush battery cap was forcibly blown off at the end of the brush handle.

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 22, 2012· Extremity Medical LLC

Recalled Item: Extremity Medical Recalled by Extremity Medical LLC Due to Lag screw...

The Issue: Lag screw measurement is short (approximately 5 mm) when using current screw...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 15, 2012· Sunquest Information Systems, Inc.

Recalled Item: Sunquest Laboratory Sunquest Laboratory is intended for use by professionals...

The Issue: Sunquest is recalling Sunquest Laboratory versions 6.1.0125 through...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 13, 2012· Advanced Sterilization Products

Recalled Item: STERRAD 200 System Carriage Recalled by Advanced Sterilization Products Due...

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

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 12, 2012· DePuy Mitek, Inc., a Johnson & Johnson Co.

Recalled Item: DePuy Mitek VAPR Hook Electrode 3.5mm Hook Electrode with Integrated...

The Issue: Product may have wrong large product identification label with symbols on...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 9, 2012· Princeton Biomeditech Corp

Recalled Item: Status Flu A + B Test Manufactured by Princeton Bio Recalled by Princeton...

The Issue: There have been reports of dual positive (Flu A + Flu B positive) results...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 9, 2012· Princeton Biomeditech Corp

Recalled Item: Poly stat Flu A & B Test Manufactured for Polymedco Recalled by Princeton...

The Issue: There have been reports of dual positive (Flu A + Flu B positive) results...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 9, 2012· Princeton Biomeditech Corp

Recalled Item: Orasure QuickFlu Rapid A+B Test Manufactured for OraSure Technologies...

The Issue: There have been reports of dual positive (Flu A + Flu B positive) results...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 8, 2012· Helix Medical LLC

Recalled Item: BLOM-SINGER indwelling TEP Occluder Recalled by Helix Medical LLC Due to...

The Issue: Helix Medical LLC is recalling the BLOM-SINGER indwelling TEP Occluder due...

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

Class III — Low RiskOngoing
Medical DeviceMarch 7, 2012· Aesculap Implant Systems LLC

Recalled Item: S4 Cervical (S4C) Revision Instruments (FW099R and FW101R). The S4C Recalled...

The Issue: Aesculap Implant Systems, LLC has initiated a voluntary removal of the S4...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 7, 2012· Abbott Point Of Care Inc.

Recalled Item: i-STAT cTnI cartridges Product Usage: The i-STAT cTnl test is Recalled by...

The Issue: Abbott Point of Care has determined that i-Stat CTNL cartridges have the...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 7, 2012· DePuy Orthopaedics, Inc.

Recalled Item: Pinnacle Hip Solutions ALTRX Polyethylene Acetabular Liner Recalled by DePuy...

The Issue: DePuy Orthopaedics, Inc. (DePuy) is issuing a voluntary recall of one lot of...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 6, 2012· GE Healthcare, LLC

Recalled Item: GE Healthcare Quasar Nuclear Medicine System Recalled by GE Healthcare, LLC...

The Issue: Accelerated fatigue of the lateral axis motion subsystem of the Infinia...

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

Class II — Potential Health HazardOngoing