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. 1,060 recalls have been distributed to West Virginia in the last 12 months.
Showing 9721–9740 of 27,884 recalls
Recalled Item: Angio Pack Recalled by Windstone Medical Packaging, Inc. Due to Angio tubing...
The Issue: Angio tubing included within Custom Convenience kits may contain...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Angio Pack Recalled by Windstone Medical Packaging, Inc. Due to Angio tubing...
The Issue: Angio tubing included within Custom Convenience kits may contain...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Revogene RNA Software Upgrade Kit Revogene RNA Software Upgrade USBs...
The Issue: Emergency Use Application (EUA) application withdrawn as false negative...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Recalled by Bard Access Systems Inc. Due to Catheters contain two issues: 1....
The Issue: Catheters contain two issues: 1. the inner diameter of the distal connector...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Recalled by Bard Access Systems Inc. Due to Catheters contain two issues: 1....
The Issue: Catheters contain two issues: 1. the inner diameter of the distal connector...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Elecsys Troponin I Immunoassay: Catalog# 05094810160 - Product Usage:...
The Issue: Recall reason is possible sporadic false negative conventional troponin...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Recalled by Bard Access Systems Inc. Due to Catheters contain two issues: 1....
The Issue: Catheters contain two issues: 1. the inner diameter of the distal connector...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Recalled by Bard Access Systems Inc. Due to Catheters contain two issues: 1....
The Issue: Catheters contain two issues: 1. the inner diameter of the distal connector...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Recalled by Bard Access Systems Inc. Due to Catheters contain two issues: 1....
The Issue: Catheters contain two issues: 1. the inner diameter of the distal connector...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Recalled by Bard Access Systems Inc. Due to Catheters contain two issues: 1....
The Issue: Catheters contain two issues: 1. the inner diameter of the distal connector...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Recalled by Bard Access Systems Inc. Due to Catheters contain two issues: 1....
The Issue: Catheters contain two issues: 1. the inner diameter of the distal connector...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Recalled by Bard Access Systems Inc. Due to Catheters contain two issues: 1....
The Issue: Catheters contain two issues: 1. the inner diameter of the distal connector...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Elecsys Troponin I STAT Immunoassay: Catalog# 05094798160 - Product Usage:...
The Issue: Recall reason is possible sporadic false negative conventional troponin...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Recalled by Bard Access Systems Inc. Due to Catheters contain two issues: 1....
The Issue: Catheters contain two issues: 1. the inner diameter of the distal connector...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Recalled by Bard Access Systems Inc. Due to Catheters contain two issues: 1....
The Issue: Catheters contain two issues: 1. the inner diameter of the distal connector...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cobalt HF Quad MRI SureScan Implantable Cardioverter Defibrillators with...
The Issue: The device may contain a manufacturing defect of a missing resistance spot...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Recalled by Bard Access Systems Inc. Due to Catheters contain two issues: 1....
The Issue: Catheters contain two issues: 1. the inner diameter of the distal connector...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Recalled by Bard Access Systems Inc. Due to Catheters contain two issues: 1....
The Issue: Catheters contain two issues: 1. the inner diameter of the distal connector...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Recalled by Bard Access Systems Inc. Due to Catheters contain two issues: 1....
The Issue: Catheters contain two issues: 1. the inner diameter of the distal connector...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Recalled by Bard Access Systems Inc. Due to Catheters contain two issues: 1....
The Issue: Catheters contain two issues: 1. the inner diameter of the distal connector...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.