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. 2,372 recalls have been distributed to West Virginia in the last 12 months.

48,376 total recalls
2,372 in last 12 months

Showing 2356123580 of 27,884 recalls

Medical DeviceJune 2, 2014· Smith & Nephew, Inc. Endoscopy Division

Recalled Item: SUTUREFIX Ultra Anchor XL with one (#2) Ultrabraid Blue Product Recalled by...

The Issue: Sterility of device is compromised due to breach in sterile barrier

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 2, 2014· Siemens Healthcare Diagnostics, Inc

Recalled Item: Siemens Healthcare ADVIA Acid/Base Reagent 1 and 2 Kit containing Recalled...

The Issue: Swollen acid bottles due to a trace metal contamination in the Acid Reagent...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 30, 2014· Instrumed International, Inc.

Recalled Item: Reusable laparoscopic instruments are packaged as non-sterile. Cleaning and...

The Issue: Additional caution statements have been added to the Instructions For Use...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 30, 2014· Instrumed International, Inc.

Recalled Item: Reusable laparoscopic instruments are packaged as non-sterile. Cleaning and...

The Issue: Additional caution statements have been added to the Instructions For Use...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 30, 2014· Instrumed International, Inc.

Recalled Item: Reusable laparoscopic instruments are packaged as non-sterile. Cleaning and...

The Issue: Additional caution statements have been added to the Instructions For Use...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 30, 2014· Carestream Health Inc.

Recalled Item: KODAK DirectView DR 9000 System Recalled by Carestream Health Inc. Due to A...

The Issue: A control system failure may cause the U-Arm to move downward unexpectedly...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 30, 2014· Instrumed International, Inc.

Recalled Item: Reusable laparoscopic instruments are packaged as non-sterile. Cleaning and...

The Issue: Additional caution statements have been added to the Instructions For Use...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 30, 2014· Instrumed International, Inc.

Recalled Item: Reusable laparoscopic instruments are packaged as non-sterile. Cleaning and...

The Issue: Additional caution statements have been added to the Instructions For Use...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 30, 2014· Instrumed International, Inc.

Recalled Item: Reusable laparoscopic instruments are packaged as non-sterile. Cleaning and...

The Issue: Additional caution statements have been added to the Instructions For Use...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 30, 2014· Alere San Diego, Inc.

Recalled Item: Alere Triage BNP Calibrators for the Beckman Coulter Access Family Recalled...

The Issue: Alere San Diego is recalling Alere Triage BNP Calibrators for the Beckman...

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

Class III — Low RiskOngoing
Medical DeviceMay 30, 2014· Instrumed International, Inc.

Recalled Item: Reusable laparoscopic instruments are packaged as non-sterile. Cleaning and...

The Issue: Additional caution statements have been added to the Instructions For Use...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 30, 2014· Siemens Healthcare Diagnostics, Inc

Recalled Item: ADVIA Centaur¿ Systems TnI-Ultra assay Recalled by Siemens Healthcare...

The Issue: The solid phase reagent in some of the ADVIA Centaur¿ TnI -Ultra...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 30, 2014· Instrumed International, Inc.

Recalled Item: Reusable laparoscopic instruments are packaged as non-sterile. Cleaning and...

The Issue: Additional caution statements have been added to the Instructions For Use...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 30, 2014· Instrumed International, Inc.

Recalled Item: Reusable laparoscopic instruments are packaged as non-sterile. Cleaning and...

The Issue: Additional caution statements have been added to the Instructions For Use...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 30, 2014· Instrumed International, Inc.

Recalled Item: Reusable laparoscopic instruments are packaged as non-sterile. Cleaning and...

The Issue: Additional caution statements have been added to the Instructions For Use...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 29, 2014· Kerr Corporation

Recalled Item: Tytin Regular Set Recalled by Kerr Corporation Due to Kerr Corporation is...

The Issue: Kerr Corporation is recalling one (1) lot of Tytin Regular Set ( Part Number...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 29, 2014· Mckesson Medical Immaging

Recalled Item: Horizon Medical Imaging Horizon Medical Imaging is a medical image Recalled...

The Issue: Firm received a complaint that an unreported study performed that day could...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 29, 2014· Elekta, Inc.

Recalled Item: iGUIDE System Product Usage: The intended use of the device Recalled by...

The Issue: A bug in the software prevents the iGUIDE software from logging off.

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 29, 2014· Synthes, Inc.

Recalled Item: Synthes Guide Blocks for the 2 Column Plate 6 Hole Recalled by Synthes, Inc....

The Issue: The Guide Blocks for the 2 Column Plate 6 Hole Head (Volar Distal Radius...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 29, 2014· Elekta, Inc.

Recalled Item: MOSAIQ MOSAIQ is an oncology information system used to manage Recalled by...

The Issue: MOSAIQ does not re-calculate the agent volume when the user changes the...

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

Class II — Potential Health HazardOngoing