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. 2,372 recalls have been distributed to West Virginia in the last 12 months.

48,376 total recalls
2,372 in last 12 months

Showing 2450124520 of 27,884 recalls

Medical DeviceDecember 12, 2013· GE Healthcare, LLC

Recalled Item: GE Healthcare Precision 500D Recalled by GE Healthcare, LLC Due to GE...

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 II — Potential Health HazardOngoing
Medical DeviceDecember 11, 2013· GE Healthcare, LLC

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

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

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 11, 2013· Toshiba American Medical Systems Inc

Recalled Item: TSX-301C Aquilion One (Vision Edition) Computed Tomography X-Ray System....

The Issue: Toshiba America Medical Systems, Inc. initiated this recall due to the...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 10, 2013· Philips Medical Systems, Inc.

Recalled Item: Philips HeartStart MRx Monitor/Defibrillator with CO2/EtCO2 Measurement The...

The Issue: MRx defibrillator displays a -?- for EtCO2 and does not display EtCO2 values...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 10, 2013· BioHorizons Implant Systems Inc

Recalled Item: External Implant RBT Recalled by BioHorizons Implant Systems Inc Due to The...

The Issue: The body length of the External Implant 40105D3 Lot 1302762 labeled as...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 9, 2013· Synergetics Inc

Recalled Item: 25ga Awh Chandelier Recalled by Synergetics Inc Due to Faulty seals on the...

The Issue: Faulty seals on the outer pouch of various, double-pouched, single-use,...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 9, 2013· Becton Dickinson & Co.

Recalled Item: BD BACTEC FX 40 instrument Recalled by Becton Dickinson & Co. Due to...

The Issue: Improperly functioning component of a diagnostic medical device may cause...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 9, 2013· Synergetics Inc

Recalled Item: 25ga Awh Chandelier Recalled by Synergetics Inc Due to Faulty seals on the...

The Issue: Faulty seals on the outer pouch of various, double-pouched, single-use,...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 9, 2013· Synergetics Inc

Recalled Item: 23ga Chow Illuminated Pick Recalled by Synergetics Inc Due to Faulty seals...

The Issue: Faulty seals on the outer pouch of various, double-pouched, single-use,...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 9, 2013· Synergetics Inc

Recalled Item: Vivid (tm) Endo Illuminator Recalled by Synergetics Inc Due to Faulty seals...

The Issue: Faulty seals on the outer pouch of various, double-pouched, single-use,...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 9, 2013· Synergetics Inc

Recalled Item: 25ga Mid-Field Endo Illuminator Recalled by Synergetics Inc Due to Faulty...

The Issue: Faulty seals on the outer pouch of various, double-pouched, single-use,...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 9, 2013· Synergetics Inc

Recalled Item: 23ga Chandelier Infusion Cannula Recalled by Synergetics Inc Due to Faulty...

The Issue: Faulty seals on the outer pouch of various, double-pouched, single-use,...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 9, 2013· Synergetics Inc

Recalled Item: Stiff 25ga Wide Field Endo Illuminator Recalled by Synergetics Inc Due to...

The Issue: Faulty seals on the outer pouch of various, double-pouched, single-use,...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 9, 2013· Synergetics Inc

Recalled Item: 23ga Mid-Field Endo Illuminator Recalled by Synergetics Inc Due to Faulty...

The Issue: Faulty seals on the outer pouch of various, double-pouched, single-use,...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 9, 2013· Gambro Renal Products, Incorporated

Recalled Item: Gambro Cartridge Blood Set Recalled by Gambro Renal Products, Incorporated...

The Issue: Occluded heparin tubing events preventing anticoagulation dosing on the...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 9, 2013· Synergetics Inc

Recalled Item: 27ga ONE-STEP (tm) Endo Illuminator Recalled by Synergetics Inc Due to...

The Issue: Faulty seals on the outer pouch of various, double-pouched, single-use,...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 9, 2013· Synergetics Inc

Recalled Item: Chandelier Infusion Cannula Recalled by Synergetics Inc Due to Faulty seals...

The Issue: Faulty seals on the outer pouch of various, double-pouched, single-use,...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 9, 2013· Synergetics Inc

Recalled Item: 25ga Awh Vivid Chandelier Recalled by Synergetics Inc Due to Faulty seals on...

The Issue: Faulty seals on the outer pouch of various, double-pouched, single-use,...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 9, 2013· Synergetics Inc

Recalled Item: Two-Port Vitrectomy (TPV (tm)) Wide Field High Flow End Irrigator Recalled...

The Issue: Faulty seals on the outer pouch of various, double-pouched, single-use,...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 9, 2013· Synergetics Inc

Recalled Item: 23ga Aspirating Endo Illuminator Recalled by Synergetics Inc Due to Faulty...

The Issue: Faulty seals on the outer pouch of various, double-pouched, single-use,...

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

Class II — Potential Health HazardOngoing