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 2110121120 of 27,884 recalls

Medical DeviceNovember 3, 2015· Ortho-Clinical Diagnostics

Recalled Item: VITROS 3600 Chemistry System Recalled by Ortho-Clinical Diagnostics Due to...

The Issue: Software anomaly may allow VITROS Systems to sample and process assays while...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 3, 2015· Ortho-Clinical Diagnostics

Recalled Item: VITROS 4600 Chemistry System Recalled by Ortho-Clinical Diagnostics Due to...

The Issue: Software anomaly may allow VITROS Systems to sample and process assays while...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 3, 2015· Diagnostic Hybrids, Inc.

Recalled Item: MicroVue SC5b-9 Plus EIA (CE-IVD) Recalled by Diagnostic Hybrids, Inc. Due...

The Issue: A component of the kit was found to contain bacterial contamination.

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

Class III — Low RiskOngoing
Medical DeviceNovember 3, 2015· Diagnostic Hybrids, Inc.

Recalled Item: MicroVue SC5b-9 Plus EIA (RUO) Recalled by Diagnostic Hybrids, Inc. Due to A...

The Issue: A component of the kit was found to contain bacterial contamination.

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

Class III — Low RiskOngoing
Medical DeviceNovember 3, 2015· Diagnostic Hybrids, Inc.

Recalled Item: MicroVue CIC-C1q EIA Recalled by Diagnostic Hybrids, Inc. Due to A component...

The Issue: A component of the kit was found to contain bacterial contamination.

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

Class III — Low RiskOngoing
Medical DeviceNovember 2, 2015· Synthes (USA) Products LLC

Recalled Item: 2.4MM locking screw SLF-TPNG with Stardrive Recess 18 mm. Intended Recalled...

The Issue: It was discovered that the above part number and lot of 2.4mm Locking Screws...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 2, 2015· Trumpf Medical Systems, Inc.

Recalled Item: Ceiling Mounted Surgical Light System TruLight 3000/5000 and Ceiling Mounted...

The Issue: The firm has received 15 complaints over ten years related to the connection...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 2, 2015· Insulet Corporation

Recalled Item: OmniPod¿ Recalled by Insulet Corporation Due to Pod's needle mechanism fails...

The Issue: Pod's needle mechanism fails to deploy or there is a delay in the deployment...

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

Class I — Serious Health HazardOngoing
Medical DeviceNovember 2, 2015· Insulet Corporation

Recalled Item: OmniPod¿ Recalled by Insulet Corporation Due to Pod's needle mechanism fails...

The Issue: Pod's needle mechanism fails to deploy or there is a delay in the deployment...

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

Class I — Serious Health HazardOngoing
Medical DeviceOctober 29, 2015· Philips Medical Systems (Cleveland) Inc

Recalled Item: Brilliance iCT SP Computed Tomography X-ray system Recalled by Philips...

The Issue: Perfusion scan feature may not be available on machines running software...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 29, 2015· Philips Medical Systems (Cleveland) Inc

Recalled Item: Brilliance 64 Computed Tomography X-ray system Recalled by Philips Medical...

The Issue: Perfusion scan feature may not be available on machines running software...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 29, 2015· NxStage Medical, Inc.

Recalled Item: NxStage System One S Cycler (High Permeability Hemodialysis System) Model...

The Issue: Ultrafiltration (UF) Volume software error inaccurate fluid removal

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 29, 2015· Philips Medical Systems (Cleveland) Inc

Recalled Item: Ingenuity CT Computed Tomography X-ray system Recalled by Philips Medical...

The Issue: Perfusion scan feature may not be available on machines running software...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 29, 2015· Philips Medical Systems (Cleveland) Inc

Recalled Item: Brilliance iCT Computed Tomography X-ray system Recalled by Philips Medical...

The Issue: Perfusion scan feature may not be available on machines running software...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 29, 2015· NxStage Medical, Inc.

Recalled Item: NxStage System One S Cycler (High Permeability Hemodialysis System) Model...

The Issue: Ultrafiltration (UF) Volume software error inaccurate fluid removal

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 29, 2015· Philips Medical Systems (Cleveland) Inc

Recalled Item: Ingenuity Core 128 Computed Tomography X-ray system Recalled by Philips...

The Issue: Perfusion scan feature may not be available on machines running software...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 29, 2015· Philips Medical Systems (Cleveland) Inc

Recalled Item: Ingenuity Core Computed Tomography X-ray system Recalled by Philips Medical...

The Issue: Perfusion scan feature may not be available on machines running software...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 28, 2015· Quest Medical, Inc.

Recalled Item: Model 5001102 MPS Delivery Set w/ arrest agent and additive cassettes...

The Issue: The products have been found to intermittently exhibit a seal failure during...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 28, 2015· Baylis Medical Corp *

Recalled Item: ProTrack Microcatheter. Model/Catalog Numbers CIC38-145 Recalled by Baylis...

The Issue: Microcatheter may have circumferential defects (cracks) along its shaft.

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 28, 2015· Implant Direct Sybron Manufacturing, LLC

Recalled Item: DGDE Recalled by Implant Direct Sybron Manufacturing, LLC Due to Implant...

The Issue: Implant Direct Sybron Manufacturing, LLC is recalling 26 lots of DGDE...

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

Class II — Potential Health HazardOngoing