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 1778117800 of 27,884 recalls

Medical DeviceApril 25, 2017· Bard Access Systems Inc.

Recalled Item: StatLock¿ IV Premium Catheter Stabilization Device Recalled by Bard Access...

The Issue: StatLockTM IV Premium Catheter Stabilization Device may contain an...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 25, 2017· BioMerieux SA

Recalled Item: ETEST ETP32 (Ertapenem) Ref. 531640 Recalled by BioMerieux SA Due to False...

The Issue: False susceptible results

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 25, 2017· Cook Inc.

Recalled Item: Pereyra Ligature Carrier 75 Recalled by Cook Inc. Due to reprocessing...

The Issue: reprocessing instructions do not provide sufficient detailed information for...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 25, 2017· Vascular Solutions, Inc.

Recalled Item: Venture RX Catheter Recalled by Vascular Solutions, Inc. Due to Vascular...

The Issue: Vascular Solutions, Inc. (VSI) is voluntarily removing all lots of Venture...

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

Class I — Serious Health HazardOngoing
Medical DeviceApril 25, 2017· Cook Inc.

Recalled Item: Endoscopic Introducer/Extractor Recalled by Cook Inc. Due to reprocessing...

The Issue: reprocessing instructions do not provide sufficient detailed information for...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 25, 2017· Cook Inc.

Recalled Item: Stamey Needle Recalled by Cook Inc. Due to reprocessing instructions do not...

The Issue: reprocessing instructions do not provide sufficient detailed information for...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 25, 2017· Cook Inc.

Recalled Item: Clarke-Reich Laparoscopic Knot Pusher Recalled by Cook Inc. Due to...

The Issue: reprocessing instructions do not provide sufficient detailed information for...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 25, 2017· Cook Inc.

Recalled Item: Pereyra-Raz Ligature Carrier Recalled by Cook Inc. Due to reprocessing...

The Issue: reprocessing instructions do not provide sufficient detailed information for...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 24, 2017· Beckman Coulter Inc.

Recalled Item: Microalbumin Reagent Recalled by Beckman Coulter Inc. Due to Beckman Coulter...

The Issue: Beckman Coulter has confirmed that MA Reagent Lot M609458 may recover...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 24, 2017· Beckman Coulter Inc.

Recalled Item: UniCel DxH 600 Coulter Cellular Analysis System Recalled by Beckman Coulter...

The Issue: There is a possibility of a data acquisition disruption that may cause an...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 24, 2017· Beckman Coulter Inc.

Recalled Item: UniCel DxH 800 Coulter Cellular Analysis System Recalled by Beckman Coulter...

The Issue: There is a possibility of a data acquisition disruption that may cause an...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 24, 2017· Respironics California Inc

Recalled Item: Philips V60 Ventilators Recalled by Respironics California Inc Due to Over...

The Issue: Over time, low-frequency vibrations can cause the pins within the female...

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

Class I — Serious Health HazardOngoing
Medical DeviceApril 24, 2017· Molnlycke Health Care, Inc

Recalled Item: Brennen Skin Graft Mesher. Surgical instrument designed to expand skin...

The Issue: Sterilization validation failure.

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 21, 2017· Cardinal Health 200, LLC

Recalled Item: Jackson-Pratt Hemaduct Silicone Round Drain Recalled by Cardinal Health 200,...

The Issue: Product's seal possibly compromised, potentially compromising the sterility...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 21, 2017· Cardinal Health 200, LLC

Recalled Item: Jackson-Pratt Silicone Flat Drain Recalled by Cardinal Health 200, LLC Due...

The Issue: Product's seal possibly compromised, potentially compromising the sterility...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 21, 2017· Cardinal Health 200, LLC

Recalled Item: Jackson-Pratt Hemaduct Silicone Round Drain Recalled by Cardinal Health 200,...

The Issue: Product's seal possibly compromised, potentially compromising the sterility...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 21, 2017· Teleflex Medical

Recalled Item: INFANT 20/BX Recalled by Teleflex Medical Due to

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 21, 2017· Cardinal Health 200, LLC

Recalled Item: Jackson-Pratt Silicone Flat Drain Recalled by Cardinal Health 200, LLC Due...

The Issue: Product's seal possibly compromised, potentially compromising the sterility...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 21, 2017· Cardinal Health 200, LLC

Recalled Item: Jackson-Pratt Silicone Round Drain Recalled by Cardinal Health 200, LLC Due...

The Issue: Product's seal possibly compromised, potentially compromising the sterility...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 21, 2017· Cardinal Health 200, LLC

Recalled Item: Jackson-Pratt Silicone Round Drain Recalled by Cardinal Health 200, LLC Due...

The Issue: Product's seal possibly compromised, potentially compromising the sterility...

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

Class II — Potential Health HazardOngoing