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. 2,380 recalls have been distributed to West Virginia in the last 12 months.

48,376 total recalls
2,380 in last 12 months

Showing 2306123080 of 27,884 recalls

Medical DeviceOctober 9, 2014· Trumpf Medical Systems, Inc.

Recalled Item: TITAN Operating Room Table Patient positioning during surgery Recalled by...

The Issue: Unintended movement of the operating table during surgical cases due to the...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 9, 2014· Siemens Healthcare Diagnostics, Inc.

Recalled Item: ADVIA Centaur (including ) Professional use in a laboratory for Recalled by...

The Issue: A slight crack of the tubing at the connecting fitting on the reservoir...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 9, 2014· Zimmer, Inc.

Recalled Item: Persona Stemmed 5 Degree Cemented Tibia Product Usage: This device Recalled...

The Issue: Cleaning process validation failure.

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 9, 2014· Siemens Healthcare Diagnostics, Inc.

Recalled Item: ADVIA Centaur XP Immunoassay System (including ) Professional use in...

The Issue: A slight crack of the tubing at the connecting fitting on the reservoir...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 8, 2014· Stryker Instruments Div. of Stryker Corporation

Recalled Item: Stryker SmartLife Large Aseptic Housing Rx Only The Recalled by Stryker...

The Issue: The SmartLife Aseptic Housings are being recalled in that the top section of...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 8, 2014· Stryker Instruments Div. of Stryker Corporation

Recalled Item: Stryker SmartLife Small Aseptic Housing Rx Only The Recalled by Stryker...

The Issue: The SmartLife Aseptic Housings are being recalled in that the top section of...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 8, 2014· Ad-Tech Medical Instrument Corporation

Recalled Item: Box Label: 3 mm Cueva Electrode Kit Recalled by Ad-Tech Medical Instrument...

The Issue: The recall has been initiated due to concerns that the applicator wand may...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 7, 2014· Zimmer, Inc.

Recalled Item: The Persona Tibial Articular Surface Inserter is a sterilizable instrument...

The Issue: Affected product did not undergo heat treatment hardening step leading to...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 7, 2014· Mako Surgical Corporation

Recalled Item: RESTORIS PST Acetabular Straight Shell Impactors An impactor is a Recalled...

The Issue: MAKO has identified the potential that the shell impactors may be damaged...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 7, 2014· Mortara Instrument, Inc

Recalled Item: Mortara Surveyor S12 and Surveyor S19 Patient Monitors. Product Usage:...

The Issue: Martara Instrument, Inc. has recently became aware of a potential safety...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 7, 2014· Mako Surgical Corporation

Recalled Item: RESTORIS PST Acetabular Offset Shell Impactors An impactor is a Recalled by...

The Issue: MAKO has identified the potential that the shell impactors may be damaged...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 7, 2014· Mako Surgical Corporation

Recalled Item: RESTORIS PST Straight Shell Inserter An impactor is a reusable Recalled by...

The Issue: MAKO has identified the potential that the shell impactors may be damaged...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 6, 2014· Zimmer Surgical Inc

Recalled Item: UNIVERSAL Modular Electric/Battery Handpiece for surgery The electric...

The Issue: Non-injury complaints from Europe identified a malfunction that made it...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 6, 2014· Mindray DS USA, Inc. dba Mindray North America

Recalled Item: DPM 6 Patient Monitor and DPM 7 Patient Monitor. The Recalled by Mindray DS...

The Issue: Mindray has identified an issue that involves the IBP module used with the...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 6, 2014· Elekta, Inc.

Recalled Item: Laksell Gamma Knife Perfexion Recalled by Elekta, Inc. Due to Elekta has...

The Issue: Elekta has become aware that the latches may be locked before they have been...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 6, 2014· PEROUSE MEDICAL

Recalled Item: Bard Caliber (CL3030) Inflation Device Product Usage: Inflation Device...

The Issue: Additional instructions for use due to inability to raise the pressure above...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 6, 2014· Siemens Healthcare Diagnostics, Inc

Recalled Item: ADVIA Centaur BNP Assay for in vitro diagnostic use in Recalled by Siemens...

The Issue: Siemens Healthcare Diagnostics has confirmed that approximately 2000...

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

Class III — Low RiskOngoing
Medical DeviceOctober 6, 2014· PEROUSE MEDICAL

Recalled Item: Synthes Inflation System (03.804.4135) Product Usage: Inflation system is...

The Issue: Additional instructions for use due to inability to raise the pressure above...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 6, 2014· Beckman Coulter Inc.

Recalled Item: UniCel DxC 600i SYNCHRON Access Clinical Analyzer Recalled by Beckman...

The Issue: Beckman Coulter is recalling the Small Form Factor Console PC (SFF PC)...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 6, 2014· Baxter Healthcare Corp.

Recalled Item: HomeChoice Automated PD system and HomeChoice Pro Automated PD system...

The Issue: There are additional and updated warning and cautions that are not in the...

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

Class II — Potential Health HazardOngoing