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. 2,404 recalls have been distributed to West Virginia in the last 12 months.

48,376 total recalls
2,404 in last 12 months

Showing 1966119680 of 27,884 recalls

Medical DeviceMay 19, 2016· Implant Direct Sybron Manufacturing, LLC

Recalled Item: 6534-08N InterActive¿ Implant Open-Tray Transfer Narrow Part Number:...

The Issue: The incorrect sized product, InterActive Implant Open-Tray Transfer Wide,...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 19, 2016· Toshiba American Medical Systems Inc

Recalled Item: Toshiba Kalare DREX-KL80 X-ray generator Recalled by Toshiba American...

The Issue: It was discovered that the generator of the system could possibly terminate...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 18, 2016· Ortho-Clinical Diagnostics

Recalled Item: VITROS Chemistry Products Ca Slides Recalled by Ortho-Clinical Diagnostics...

The Issue: Ortho Clinical Diagnostics (OCD) confirmed a potential for biased calcium...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 18, 2016· Conmed Corporation

Recalled Item: Adult Dual Dispersive Electrodes (for patients >15 kg.) Recalled by Conmed...

The Issue: A version of the dual dispersive electrodes may not be compatible with some...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 18, 2016· Conmed Corporation

Recalled Item: Pediatric ThermoGard¿ Dual Dispersive Electrodes (for patients 5-15 kg.)...

The Issue: A version of the dual dispersive electrodes may not be compatible with some...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 18, 2016· Conmed Corporation

Recalled Item: Adult ThermoGard¿ Dual Dispersive Electrodes (for patients >15 kg.) Recalled...

The Issue: A version of the dual dispersive electrodes may not be compatible with some...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 18, 2016· Conmed Corporation

Recalled Item: Pediatric Dual Dispersive Electrodes (for patients 5-15 kg.) Recalled by...

The Issue: A version of the dual dispersive electrodes may not be compatible with some...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 18, 2016· Conmed Corporation

Recalled Item: Adult ThermoGard¿ Dual Dispersive Electrodes (for patients >15 kg.) Recalled...

The Issue: A version of the dual dispersive electrodes may not be compatible with some...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 18, 2016· Elekta, Inc.

Recalled Item: Monaco RTP System Product Usage: The Monaco system is used Recalled by...

The Issue: When DICOM exporting a 3D Monaco plan and the "Composite Field Sequencing"...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 17, 2016· X Spine Systems Inc

Recalled Item: Calix P PEEK Lumbar System Recalled by X Spine Systems Inc Due to The trials...

The Issue: The trials and rasps used to prepare the surgical site for placement of the...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 17, 2016· CSL Behring GmbH

Recalled Item: Dimension Vista¿ Homocysteine Flex Reagent Cartridge (HCYS) Recalled by CSL...

The Issue: Reagent lots # 15243MA and 15243MB shows a reduced stability once opened...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 17, 2016· Carefusion 211 Inc dba Carefusion

Recalled Item: Gas Delivery Engine (GDE) Recalled by Carefusion 211 Inc dba Carefusion Due...

The Issue: CareFusion has identified a potential risk associated with AVEA Ventilator...

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

Class I — Serious Health HazardOngoing
Medical DeviceMay 17, 2016· Carefusion 211 Inc dba Carefusion

Recalled Item: AVEA Standard with Compressor ventilator- Recalled by Carefusion 211 Inc dba...

The Issue: CareFusion has identified a potential risk associated with AVEA Ventilator...

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

Class I — Serious Health HazardOngoing
Medical DeviceMay 17, 2016· Carefusion 211 Inc dba Carefusion

Recalled Item: AVEA Standard with Compressor ventilator Recalled by Carefusion 211 Inc dba...

The Issue: CareFusion has identified a potential risk associated with AVEA Ventilator...

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

Class I — Serious Health HazardOngoing
Medical DeviceMay 17, 2016· Carefusion 211 Inc dba Carefusion

Recalled Item: AVEA Comprehensive ventilator Recalled by Carefusion 211 Inc dba Carefusion...

The Issue: CareFusion has identified a potential risk associated with AVEA Ventilator...

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

Class I — Serious Health HazardOngoing
Medical DeviceMay 17, 2016· Carefusion 211 Inc dba Carefusion

Recalled Item: AVEA Standard ventilator- Recalled by Carefusion 211 Inc dba Carefusion Due...

The Issue: CareFusion has identified a potential risk associated with AVEA Ventilator...

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

Class I — Serious Health HazardOngoing
Medical DeviceMay 17, 2016· Carefusion 211 Inc dba Carefusion

Recalled Item: AVEA GDE/UIM upgrade kit Recalled by Carefusion 211 Inc dba Carefusion Due...

The Issue: CareFusion has identified a potential risk associated with AVEA Ventilator...

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

Class I — Serious Health HazardOngoing
Medical DeviceMay 17, 2016· Carefusion 211 Inc dba Carefusion

Recalled Item: TCA Board Recalled by Carefusion 211 Inc dba Carefusion Due to CareFusion...

The Issue: CareFusion has identified a potential risk associated with AVEA Ventilator...

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

Class I — Serious Health HazardOngoing
Medical DeviceMay 17, 2016· X Spine Systems Inc

Recalled Item: Calix T PEEK Lumbar System Recalled by X Spine Systems Inc Due to The trials...

The Issue: The trials and rasps used to prepare the surgical site for placement of the...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 17, 2016· Carefusion 211 Inc dba Carefusion

Recalled Item: AVEA Comprehensive ventilator- Recalled by Carefusion 211 Inc dba Carefusion...

The Issue: CareFusion has identified a potential risk associated with AVEA Ventilator...

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

Class I — Serious Health HazardOngoing