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. 2,393 recalls have been distributed to West Virginia in the last 12 months.

48,376 total recalls
2,393 in last 12 months

Showing 2242122440 of 27,884 recalls

Medical DeviceFebruary 4, 2015· Fujifilm Medical Systems U.S.A., Inc.

Recalled Item: Fujifilm Synapse Cardiovascular I ProSolv CardioVascular Synapse...

The Issue: Under certain circumstances the patient Demographics in a report exported...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 3, 2015· Philips Medical Systems, Inc.

Recalled Item: Philips Healthcare Xper cardio systems Model : 722123 Product Usage:...

The Issue: Monitor Ceiling Suspension system may fall

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 3, 2015· Philips Medical Systems, Inc.

Recalled Item: Philips Healthcare Allura Xper Series: Allura Xper FD10 Allura Xper Recalled...

The Issue: Monitor Ceiling Suspension system may fall

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 3, 2015· Philips Medical Systems, Inc.

Recalled Item: Philips Healthcare INTEGRIS H5000F/Allura 9F Model : 722017 Product Usage:...

The Issue: Monitor Ceiling Suspension system may fall

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 3, 2015· Philips Medical Systems, Inc.

Recalled Item: Philips Healthcare Xper vascular systems R7.6 Model : 722134 Product...

The Issue: Monitor Ceiling Suspension system may fall

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 3, 2015· Philips Medical Systems, Inc.

Recalled Item: Philips Healthcare INTEGRIS vascular System Model : 722122 Product Usage:...

The Issue: Monitor Ceiling Suspension system may fall

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 3, 2015· Philips Medical Systems, Inc.

Recalled Item: Philips Healthcare INTEGRIS cardio system Model : 722121 Product Usage:...

The Issue: Monitor Ceiling Suspension system may fall

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 3, 2015· Philips Medical Systems, Inc.

Recalled Item: Philips Healthcare Xper vascular system Model : 722124 Product Usage:...

The Issue: Monitor Ceiling Suspension system may fall

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 3, 2015· Philips Medical Systems, Inc.

Recalled Item: Philips Healthcare Xper cardio systems R7.6 Model : 722133 Product Recalled...

The Issue: Monitor Ceiling Suspension system may fall

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 3, 2015· Philips Medical Systems, Inc.

Recalled Item: Philips Healthcare Allure BiPlane Series: Model 722013 Allura Xper FD20...

The Issue: Monitor Ceiling Suspension system may fall

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 3, 2015· Norwex Usa Inc

Recalled Item: Manual Toothbrush Recalled by Norwex Usa Inc Due to The toothbrush head can...

The Issue: The toothbrush head can potentially disengage from the handle.

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 3, 2015· Synthes, Inc.

Recalled Item: Synthes Inserter for Titanium Elastic Nails Recalled by Synthes, Inc. Due to...

The Issue: The Inserter has the potential for mechanical failures such as breakage of...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 2, 2015· Microport Orthopedics INC.

Recalled Item: EVOLUTION MP TIBIAL BASE Recalled by Microport Orthopedics INC. Due to Some...

The Issue: Some units of the EVOLUTION Tibial Base was affected by a casting tool issue...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 2, 2015· Smiths Medical ASD, Inc.

Recalled Item: CADD" Medication Cassette Reservoir Recalled by Smiths Medical ASD, Inc. Due...

The Issue: Smiths Medical has become aware of an issue with specific lots of 50mL CADD"...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 2, 2015· Bradshaw Medical Inc.

Recalled Item: Axial Torque Limiting Driver (1st generation) Product Usage: The Bradshaw...

The Issue: A component failure could cause a situation where the applied torque was...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 2, 2015· Invacare Corporation

Recalled Item: Invacare¿ Pronto¿ Air Personal Transporter (power wheelchair) Recalled by...

The Issue: The batteries used in the Invacare¿ Pronto¿ Air Personal Transporter models...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 30, 2015· GE Healthcare

Recalled Item: GE Healthcare Proteus XR/a with wall stand model number 2260354. Recalled by...

The Issue: Potential breakage of the steel cable which supports the bucky device in...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 30, 2015· Penner Mfg Inc

Recalled Item: Penner Patient Stretcher/Transfer Lift System Models 391000-1 and 392000-1...

The Issue: If the patient sits on either wing, not squarely on the center section of...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 30, 2015· Maquet Datascope Corp - Cardiac Assist Division

Recalled Item: Maquet CARDIOSAVE Hybrid Intra-Aortic Balloon Pump (IABP) Recalled by Maquet...

The Issue: Power supply malfunction complaints related to suboptimal thermal management.

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 30, 2015· C.R. Bard, Inc.

Recalled Item: Bard 100% Latex-Free Urinary Drainage Bag with Anti- Chamber and Recalled by...

The Issue: Potential breach of the sterile barrier packaging.

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

Class II — Potential Health HazardOngoing