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. 2,455 recalls have been distributed to West Virginia in the last 12 months.

48,376 total recalls
2,455 in last 12 months

Showing 1710117120 of 27,884 recalls

Medical DeviceJuly 13, 2017· Medtronic Vascular Galway DBA Medtronic Ireland

Recalled Item: Euphora Rapid Exchange Balloon Dilatation Catheter Recalled by Medtronic...

The Issue: Stylette removal difficulties on the Euphora and Solarice products.

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 11, 2017· Olympus Scientific Solutions Americas

Recalled Item: Olympus Scientific Solutions Americas Corporation (OSSA) Model: VANTA...

The Issue: Instruments may, under certain specific circumstances listed below, fail to...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 11, 2017· Philips Medical Systems (Cleveland) Inc

Recalled Item: Brilliance iCT SP - Model 728311 Brilliance iCT - Model Recalled by Philips...

The Issue: Numerous software issues with Brilliance iCT 4.1.6 version. Issues affect...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 11, 2017· Philips Medical Systems (Cleveland) Inc

Recalled Item: Brilliance iCT - Model 728306 Computed Tomography X-ray systems Recalled by...

The Issue: Numerous software issues with Brilliance iCT 4.1.6 version. Issues affect...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 7, 2017· Ondamed Inc

Recalled Item: Ondamed Biofeedback Device Recalled by Ondamed Inc Due to The firm was...

The Issue: The firm was marketing the Ondamed System in the US without marketing...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 7, 2017· Qualigen Inc

Recalled Item: Qualigen(R) The FastPack(R) IP Vitamin D Complete Immunoassay Kit Recalled...

The Issue: Specific lots have been reported to produce falsely lower than expected...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 6, 2017· Edwards Lifesciences, LLC

Recalled Item: Fogarty Adherent Clot Catheter Model Numbers 1408010 and 140806 Product...

The Issue: The diameter of the Fogarty Catheter balloon, measures 6mm instead of 10mm.

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 5, 2017· Cosman Medical, LLC

Recalled Item: Nitinol TC Reusable Electrodes (TCN) Recalled by Cosman Medical, LLC Due to...

The Issue: After multiple reprocessing cycles, the epoxy resin which holds the TCN...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 5, 2017· Teleflex Medical

Recalled Item: LMA(TM) MADgic(TM) Laryngo-Tracheal Mucosal Atomization Devices: (a) MAD600...

The Issue: Teleflex Medical is recalling the affected product because there may be...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 5, 2017· Roche Diagnostics Corporation

Recalled Item: cobas e 411 Immunoassay Analyzer-Model/Catalog/Part number:...

The Issue: A software malfunction can occur on the cobas e 411 and Elecsys 2010...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 5, 2017· Novo Nordisk Inc

Recalled Item: Dial-A-Dose Insulin Delivery Device (Pen-Injector) cartridge holders Product...

The Issue: A small number of batches may crack or break if exposed to certain...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 5, 2017· Phadia US Inc

Recalled Item: Phadia 1000 Instrument Recalled by Phadia US Inc Due to The "Retry" command...

The Issue: The "Retry" command does not function properly which could cause a shortage...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 5, 2017· Roche Diagnostics Corporation

Recalled Item: Roche / Hitachi MODULAR Analyzer Systems-Immunoassay...

The Issue: A software malfunction can occur on the cobas e 411 and Elecsys 2010...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 30, 2017· Sorin Group USA, Inc.

Recalled Item: STOCKERT Heater-Cooler System 3T Recalled by Sorin Group USA, Inc. Due to...

The Issue: Plastic heat exchanger fibers separating the blood compartment from the...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 30, 2017· Sorin Group USA, Inc.

Recalled Item: STOCKERT Heater-Cooler System 3T Recalled by Sorin Group USA, Inc. Due to...

The Issue: Plastic heat exchanger fibers separating the blood compartment from the...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 30, 2017· Sorin Group USA, Inc.

Recalled Item: STOCKERT Heater-Cooler System 3T Recalled by Sorin Group USA, Inc. Due to...

The Issue: Plastic heat exchanger fibers separating the blood compartment from the...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 30, 2017· Sorin Group USA, Inc.

Recalled Item: STOCKERT Heater-Cooler System 3T Recalled by Sorin Group USA, Inc. Due to...

The Issue: Plastic heat exchanger fibers separating the blood compartment from the...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 30, 2017· Sorin Group USA, Inc.

Recalled Item: STOCKERT Heater-Cooler System 3T Recalled by Sorin Group USA, Inc. Due to...

The Issue: Plastic heat exchanger fibers separating the blood compartment from the...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 30, 2017· R82 A/S

Recalled Item: Heron toilet and bath chair Model 880505-01 & 880505-11 Recalled by R82 A/S...

The Issue: Replacement campaign on all units that have a gas spring head in aluminum.

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 30, 2017· Alcon Research, Ltd.

Recalled Item: ORA System with VerifEye+ Cart Recalled by Alcon Research, Ltd. Due to Some...

The Issue: Some ORA Carts have the potential to return an incorrect IOL power...

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

Class II — Potential Health HazardOngoing