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 2714127160 of 27,884 recalls

Medical DeviceJune 22, 2012· Terumo Cardiovascular Systems Corporation

Recalled Item: System 1 Base 220/240V The Terumo¿ Advanced Perfusion System 1 Recalled by...

The Issue: Terumo Cardiovascular Systems (Terumo CVS) received eight complaints since...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 22, 2012· Terumo Cardiovascular Systems Corporation

Recalled Item: System 1 Base Recalled by Terumo Cardiovascular Systems Corporation Due to...

The Issue: Terumo Advanced Perfusion System 1 battery charge is being depleted faster...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 22, 2012· Terumo Cardiovascular Systems Corporation

Recalled Item: Central Control Module for System 1: System 1 Base Recalled by Terumo...

The Issue: Terumo CVS has received reports of the Central Control Monitor (CCM) for...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 22, 2012· Terumo Cardiovascular Systems Corporation

Recalled Item: Terumo Advanced Perfusion System 1 System 1 Base Recalled by Terumo...

The Issue: Terumo Cardiovascular Systems (Terumo CVS) received two complaints related...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 22, 2012· Terumo Cardiovascular Systems Corporation

Recalled Item: Terumo Advanced Perfusion System 1 Electronic O2 Blender/Analyzer. The...

The Issue: Terumo Cardiovascular Systems (Terumo CVS) received two complaints related...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 22, 2012· Terumo Cardiovascular Systems Corporation

Recalled Item: System 1 Base Recalled by Terumo Cardiovascular Systems Corporation Due to...

The Issue: Terumo Advanced Perfusion System 1 battery charge is being depleted faster...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 22, 2012· Terumo Cardiovascular Systems Corporation

Recalled Item: Central Control Module for System 1: System 1 Base Recalled by Terumo...

The Issue: Terumo CVS has received reports of the Central Control Monitor (CCM) for...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 22, 2012· Terumo Cardiovascular Systems Corporation

Recalled Item: Terumo Advanced Perfusion System 1 System 1 Base Recalled by Terumo...

The Issue: Terumo Cardiovascular Systems (Terumo CVS) received two complaints related...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 21, 2012· Terumo Cardiovascular Systems Corporation

Recalled Item: System 1 Base Recalled by Terumo Cardiovascular Systems Corporation Due to...

The Issue: Terumo¿ Advanced Perfusion System 1 has displayed a Red X error message on...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 21, 2012· Terumo Cardiovascular Systems Corporation

Recalled Item: Terumo Advanced Perfusion System 1 System 1 Base Recalled by Terumo...

The Issue: Terumo Cardiovascular Systems has received reports of several issues that...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 21, 2012· Terumo Cardiovascular Systems Corporation

Recalled Item: Terumo Advanced Perfusion System 1 System 1 Base Recalled by Terumo...

The Issue: Terumo Cardiovascular Systems has received reports of several issues that...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 21, 2012· Terumo Cardiovascular Systems Corporation

Recalled Item: System 1 Base Recalled by Terumo Cardiovascular Systems Corporation Due to...

The Issue: Terumo¿ Advanced Perfusion System 1 has displayed a Red X error message on...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 21, 2012· Elekta, Inc.

Recalled Item: Focal SIM Planning of radiation therapy Recalled by Elekta, Inc. Due to...

The Issue: Incorrect patient shift directions when the Setup dialog is printed out when...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 21, 2012· Elekta, Inc.

Recalled Item: Monaco Product Usage: Planning of radiation therapy Recalled by Elekta, Inc....

The Issue: Incorrect patient shift directions when the Setup dialog is printed out when...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 20, 2012· Gulf South Medical Supply Inc

Recalled Item: Select Medical Products Vinyl Powder-Free Exam Gloves Recalled by Gulf South...

The Issue: Gulf South Medical Supply recalled their Select Medium and Large size Vinyl...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 20, 2012· Terumo Cardiovascular Systems Corporation

Recalled Item: System 8000 Base Product Usage: The Sarns Modular Perfusion System Recalled...

The Issue: During a retrospective review of complaint events, TCVS identified on...

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

Class III — Low RiskOngoing
Medical DeviceJune 20, 2012· Philips Healthcare Inc.

Recalled Item: Philips HeartStart MRx monitor/defibrillators Models: M3535A and M3536A...

The Issue: Therapy Cable Connection wear may lead to a malfunction in detection of...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 20, 2012· Philips Healthcare Inc.

Recalled Item: Philips HeartStart MRx monitor/defibrillators Models: M3535A Recalled by...

The Issue: HeartStart MRx Unexpected Pads/Paddles ECG Failure

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 20, 2012· Siemens Medical Solutions USA, Inc

Recalled Item: Siemens syngo.plaza Radiological Image Processing System Usage: Radiological...

The Issue: Firm has become aware of an unintended behavior when using syngo.plaza and...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 19, 2012· Eos Imaging Inc

Recalled Item: EOS X-ray Medical Diagnostic Recalled by Eos Imaging Inc Due to It was...

The Issue: It was discovered of several generator failures of the EOS System due to...

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

Class II — Potential Health HazardOngoing