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. 989 recalls have been distributed to West Virginia in the last 12 months.

48,376 total recalls
989 in last 12 months

Showing 20401–20420 of 48,376 recalls

Medical DeviceAugust 15, 2019· Zimmer Biomet, Inc.

Recalled Item: XP-XP Tibial Tray - Interlok 63 mm Item # 195751 Recalled by Zimmer Biomet,...

The Issue: The locking bar not fully engaging

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 15, 2019· Zimmer Biomet, Inc.

Recalled Item: Vanguard XP Tibial Tray 87 mm Item # 195254 Recalled by Zimmer Biomet, Inc....

The Issue: The locking bar not fully engaging

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 15, 2019· Siemens Healthcare Diagnostics, Inc.

Recalled Item: Atellica IM 1600 Analyzer Recalled by Siemens Healthcare Diagnostics, Inc....

The Issue: Issues Scanning New Reagent Lot Test Definition on the Atellica IM 1300...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 15, 2019· Zimmer Biomet, Inc.

Recalled Item: XP-XP Tibial Tray - Interlok 67 mm Item # 195753 Recalled by Zimmer Biomet,...

The Issue: The locking bar not fully engaging

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 15, 2019· Zimmer Biomet, Inc.

Recalled Item: XP-CR Tibial Tray - Interlok 83 mm Item # 195277 Recalled by Zimmer Biomet,...

The Issue: The locking bar not fully engaging

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 15, 2019· Zimmer Biomet, Inc.

Recalled Item: Vanguard XP Tibial Tray 83 mm Item # 195253 Recalled by Zimmer Biomet, Inc....

The Issue: The locking bar not fully engaging

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 15, 2019· Zimmer Biomet, Inc.

Recalled Item: XP-CR Tibial Tray - Interlok 91 mm Item # 195279 Recalled by Zimmer Biomet,...

The Issue: The locking bar not fully engaging

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 15, 2019· Zimmer Biomet, Inc.

Recalled Item: Vanguard XP Tibial Tray 75 mm Item # 195251 Recalled by Zimmer Biomet, Inc....

The Issue: The locking bar not fully engaging

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 15, 2019· Zimmer Biomet, Inc.

Recalled Item: XP-CR Tibial Tray - Porous Plasma 91 mm Item # 195291 Recalled by Zimmer...

The Issue: The locking bar not fully engaging

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 15, 2019· Zimmer Biomet, Inc.

Recalled Item: XP-CR Tibial Tray - Interlok 63mm Item # 195269 Recalled by Zimmer Biomet,...

The Issue: The locking bar not fully engaging

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 15, 2019· Zimmer Biomet, Inc.

Recalled Item: XP-XP Tibial Tray - Interlok 69 mm Item # 195754 Recalled by Zimmer Biomet,...

The Issue: The locking bar not fully engaging

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 15, 2019· Zimmer Biomet, Inc.

Recalled Item: XP-CR Tibial Tray - Interlok 69mm Item # 195272 Recalled by Zimmer Biomet,...

The Issue: The locking bar not fully engaging

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 15, 2019· Zimmer Biomet, Inc.

Recalled Item: XP-CR Tibial Tray - Interlok 79 mm Item # 195276 Recalled by Zimmer Biomet,...

The Issue: The locking bar not fully engaging

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 15, 2019· Normand-Info S.A.S.U.

Recalled Item: Remisol Advance running on hardware with Windows XP Recalled by Normand-Info...

The Issue: A patch was released for a critical remote code execution vulnerability in...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 15, 2019· Zimmer Biomet, Inc.

Recalled Item: XP-CR Tibial Tray - Interlok 73mm Item # 195274 Recalled by Zimmer Biomet,...

The Issue: The locking bar not fully engaging

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 15, 2019· Zimmer Biomet, Inc.

Recalled Item: XP-XP Tibial Tray - Interlok 91mm Item # 195761 Recalled by Zimmer Biomet,...

The Issue: The locking bar not fully engaging

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 15, 2019· Zimmer Biomet, Inc.

Recalled Item: XP-CR Tibial Tray - Interlok 75mm Item # 195275 Recalled by Zimmer Biomet,...

The Issue: The locking bar not fully engaging

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 15, 2019· Zimmer Biomet, Inc.

Recalled Item: XP-XP Tibial Tray - Interlok 83 mm Item # 195759 Recalled by Zimmer Biomet,...

The Issue: The locking bar not fully engaging

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 15, 2019· Siemens Healthcare Diagnostics, Inc.

Recalled Item: Atellica IM 1300 Analyzer Recalled by Siemens Healthcare Diagnostics, Inc....

The Issue: Issues Scanning New Reagent Lot Test Definition on the Atellica IM 1300...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 15, 2019· Western / Scott Fetzer Company

Recalled Item: Grab n Go Opti series VIPR system Model # PRX-9632 Recalled by Western /...

The Issue: Limited access to flow settings as a result of the control knob having been...

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

Class II — Potential Health HazardOngoing