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 2176121780 of 27,884 recalls

Medical DeviceMay 8, 2015· Stryker Instruments Div. of Stryker Corporation

Recalled Item: 0210-312-000-Woundcare Replacement kit with soft tip Recalled by Stryker...

The Issue: Potential sterility breach in the packaging.

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 8, 2015· Ethicon, Inc.

Recalled Item: Ethicon Fast Absorbing Plain Gut - MultiPass Needles Recalled by Ethicon,...

The Issue: Ethicon Fast Absorbing Surgical Gut (Plain) Suture is being recalled because...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 8, 2015· RAYSEARCH LABORATORIES AB

Recalled Item: RaySearch RayStation 2.5 Recalled by RAYSEARCH LABORATORIES AB Due to...

The Issue: RaySearch Laboratories AB became aware of an issue with the dose calculation...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 8, 2015· Gyrus Acmi, Incorporated

Recalled Item: Gyrus ACMI Diego Elite Tubeset Recalled by Gyrus Acmi, Incorporated Due to...

The Issue: Potential lack of sterility assurance.

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 7, 2015· Atrium Medical Corporation

Recalled Item: Ocean Water Seal Chest Drain Recalled by Atrium Medical Corporation Due to...

The Issue: Chest drains have a missing o-ring

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 7, 2015· Roche Diagnostics Operations, Inc.

Recalled Item: HDL-Cholesterol gen.3. For the quantitative determination of high-density...

The Issue: Possible drug interference when using the Trinder reaction method on...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 7, 2015· Roche Diagnostics Operations, Inc.

Recalled Item: Creatinine Plus ver. 2. Intended for use on COBAS INTEGRA systems Recalled...

The Issue: Possible drug interference when using the Trinder reaction method on...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 7, 2015· Atrium Medical Corporation

Recalled Item: Ocean Water Seal Chest Drain Recalled by Atrium Medical Corporation Due to...

The Issue: Chest drains have a missing o-ring

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 7, 2015· Roche Diagnostics Operations, Inc.

Recalled Item: HDL-Cholesterol plus gen.3. Recalled by Roche Diagnostics Operations, Inc....

The Issue: Possible drug interference when using the Trinder reaction method on...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 7, 2015· Roche Diagnostics Operations, Inc.

Recalled Item: Uric Acid plus ver.2 In vitro test for the quantitative Recalled by Roche...

The Issue: Possible drug interference when using the Trinder reaction method on...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 7, 2015· Roche Diagnostics Operations, Inc.

Recalled Item: Triglycerides/Glycerol Blanked. In vitro test for the quantitative...

The Issue: Possible drug interference when using the Trinder reaction method on...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 7, 2015· Roche Diagnostics Operations, Inc.

Recalled Item: Creatinine Plus. Intended for use on Hitachi/MODULAR systems for the...

The Issue: Possible drug interference when using the Trinder reaction method on...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 7, 2015· Atrium Medical Corporation

Recalled Item: EXPRESS Dry Seal Chest Drain Recalled by Atrium Medical Corporation Due to...

The Issue: Chest drains have a missing o-ring

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 7, 2015· Roche Diagnostics Operations, Inc.

Recalled Item: Lactate. Intended for use on COBAS INTEGRA 800 and 400 plus systems Recalled...

The Issue: Possible drug interference when using the Trinder reaction method on...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 7, 2015· Atrium Medical Corporation

Recalled Item: Oasis Dry Suction Water Seal Chest Drain Recalled by Atrium Medical...

The Issue: Chest drains have a missing o-ring

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 7, 2015· Roche Diagnostics Operations, Inc.

Recalled Item: LDL-Cholesterol plus gen.2. The Boehringer Mannheim Direct LDL-Cholesterol...

The Issue: Possible drug interference when using the Trinder reaction method on...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 7, 2015· Roche Diagnostics Operations, Inc.

Recalled Item: Cholesterol Gen.2. The cassette COBAS Integra Cholesterol Gen.2 (CHOL2)...

The Issue: Possible drug interference when using the Trinder reaction method on...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 7, 2015· Roche Diagnostics Operations, Inc.

Recalled Item: LDL-Cholesterol gen.2. The Boehringer Mannheim Direct LDL-Cholesterol test...

The Issue: Possible drug interference when using the Trinder reaction method on...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 7, 2015· Roche Diagnostics Operations, Inc.

Recalled Item: Cholesterol CHOD-PAP. In vitro diagnostic reagent system intended for use...

The Issue: Possible drug interference when using the Trinder reaction method on...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 7, 2015· Roche Diagnostics Operations, Inc.

Recalled Item: Triglycerides GPO. In vitro test for the quantitative determination of...

The Issue: Possible drug interference when using the Trinder reaction method on...

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

Class II — Potential Health HazardOngoing