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. 2,492 recalls have been distributed to West Virginia in the last 12 months.

48,376 total recalls
2,492 in last 12 months

Showing 1308113100 of 27,884 recalls

Medical DeviceAugust 1, 2019· Rocket Medical Plc

Recalled Item: Rocket KCH Fetal Bladder Drainage Catheter Model: R57405 Recalled by Rocket...

The Issue: A complaint was received regarding kinking of the device prior to use. If a...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 1, 2019· GN Otometrics

Recalled Item: Gold Cup Leadwire and Snap Leadwire with the following component Recalled by...

The Issue: The electrode lead connector has a protruding conductor beyond insulation of...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 31, 2019· Becton Dickinson & Company

Recalled Item: BD Vacutainer¿ Push Button Blood Collection Set with Pre-Attached Holder...

The Issue: Separation of front and rear barrels upon activation of the safety feature...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 31, 2019· Stryker Instruments Div. of Stryker Corporation

Recalled Item: C2 Nerve Monitor Recalled by Stryker Instruments Div. of Stryker Corporation...

The Issue: Stryker C2 NerveMonitor's design and instructions may not optimally address...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 31, 2019· Stryker Instruments Div. of Stryker Corporation

Recalled Item: C2 Nerve Monitor Recalled by Stryker Instruments Div. of Stryker Corporation...

The Issue: Stryker C2 NerveMonitor's design and instructions may not optimally address...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 31, 2019· Siemens Medical Solutions USA, Inc

Recalled Item: SOMATOM go.Top Recalled by Siemens Medical Solutions USA, Inc Due to The...

The Issue: The injector holder could potentially fall off together with the injector...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 31, 2019· Siemens Medical Solutions USA, Inc

Recalled Item: SOMATOM go.Top Recalled by Siemens Medical Solutions USA, Inc Due to The...

The Issue: The injector holder could potentially fall off together with the injector...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 31, 2019· Siemens Medical Solutions USA, Inc

Recalled Item: SOMATOM go.Now Recalled by Siemens Medical Solutions USA, Inc Due to The...

The Issue: The injector holder could potentially fall off together with the injector...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 31, 2019· Siemens Medical Solutions USA, Inc

Recalled Item: SOMATOM go.All Recalled by Siemens Medical Solutions USA, Inc Due to The...

The Issue: The injector holder could potentially fall off together with the injector...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 31, 2019· Siemens Medical Solutions USA, Inc

Recalled Item: SOMATOM go.Up Recalled by Siemens Medical Solutions USA, Inc Due to The...

The Issue: The injector holder could potentially fall off together with the injector...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 31, 2019· Siemens Medical Solutions USA, Inc

Recalled Item: SOMATOM go.Up Recalled by Siemens Medical Solutions USA, Inc Due to The...

The Issue: The injector holder could potentially fall off together with the injector...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 31, 2019· Siemens Medical Solutions USA, Inc

Recalled Item: SOMATOM go.All Recalled by Siemens Medical Solutions USA, Inc Due to The...

The Issue: The injector holder could potentially fall off together with the injector...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 30, 2019· Shanghai United Imaging Healthcare Co., Ltd.

Recalled Item: Digital Medical X-ray Imaging System Recalled by Shanghai United Imaging...

The Issue: X-ray imaging system positioning image and protocol label is reversed for...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 30, 2019· Eizo Corporation

Recalled Item: RadiForce GX560 monochrome LCD monitor Recalled by Eizo Corporation Due to...

The Issue: Under certain conditions, a marble pattern infrequently appears on the monitor.

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 30, 2019· Eizo Corporation

Recalled Item: RadiForce RX360 Recalled by Eizo Corporation Due to Under certain...

The Issue: Under certain conditions, a marble pattern infrequently appears on the monitor.

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 30, 2019· Siemens Healthcare Diagnostics, Inc.

Recalled Item: Siemens Atellica CH 930 Analyzer. Siemens Material Number (SMN): 11067000...

The Issue: Atellica CH 930 Analyzer - Erroneous Indices for Hemolysis and Lipemia in...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 30, 2019· Teleflex Medical

Recalled Item: Hudson RCI Sheridan/CF: a) 3.0 mm Recalled by Teleflex Medical Due to...

The Issue: Reported complaints indicate an increased incidence of specific lots of the...

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

Class I — Serious Health HazardOngoing
Medical DeviceJuly 30, 2019· Teleflex Medical

Recalled Item: Hudson RCI Sheridan EZ-ENDO: a) 5.0 mm Recalled by Teleflex Medical Due to...

The Issue: Reported complaints indicate an increased incidence of specific lots of the...

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

Class I — Serious Health HazardOngoing
Medical DeviceJuly 30, 2019· Teleflex Medical

Recalled Item: Hudson RCI Sheridan/HVT: a) 5.0 mm Recalled by Teleflex Medical Due to...

The Issue: Reported complaints indicate an increased incidence of specific lots of the...

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

Class I — Serious Health HazardOngoing
Medical DeviceJuly 30, 2019· Teleflex Medical

Recalled Item: Hudson RCI Sheridan Preformed: a) 3.0 mm Recalled by Teleflex Medical Due to...

The Issue: Reported complaints indicate an increased incidence of specific lots of the...

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

Class I — Serious Health HazardOngoing