Product Recalls in Virginia

Product recalls affecting Virginia — including food, drugs, consumer products, medical devices, and vehicles distributed to Virginia. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 2,803 recalls have been distributed to Virginia in the last 12 months.

53,829 total recalls
2,803 in last 12 months

Showing 99419960 of 29,425 recalls

Medical DeviceApril 7, 2021· Bard Access Systems Inc.

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.

Class II — Potential Health HazardOngoing
Medical DeviceApril 7, 2021· Bard Access Systems Inc.

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.

Class II — Potential Health HazardOngoing
Medical DeviceApril 7, 2021· Bard Access Systems Inc.

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.

Class II — Potential Health HazardOngoing
Medical DeviceApril 7, 2021· Roche Diagnostics Operations, Inc.

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.

Class II — Potential Health HazardOngoing
Medical DeviceApril 7, 2021· Bard Access Systems Inc.

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.

Class II — Potential Health HazardOngoing
Medical DeviceApril 7, 2021· Bard Access Systems Inc.

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.

Class II — Potential Health HazardOngoing
Medical DeviceApril 7, 2021· Bard Access Systems Inc.

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.

Class II — Potential Health HazardOngoing
Medical DeviceApril 7, 2021· Bard Access Systems Inc.

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.

Class II — Potential Health HazardOngoing
Medical DeviceApril 7, 2021· Bard Access Systems Inc.

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.

Class II — Potential Health HazardOngoing
Medical DeviceApril 7, 2021· Bard Access Systems Inc.

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.

Class II — Potential Health HazardOngoing
Medical DeviceApril 7, 2021· Roche Diagnostics Operations, Inc.

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.

Class II — Potential Health HazardOngoing
Medical DeviceApril 7, 2021· Bard Access Systems Inc.

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.

Class II — Potential Health HazardOngoing
Medical DeviceApril 7, 2021· Medtronic Inc., Cardiac Rhythm and Heart Failure (CRHF)

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.

Class II — Potential Health HazardOngoing
Medical DeviceApril 7, 2021· Bard Access Systems Inc.

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.

Class II — Potential Health HazardOngoing
Medical DeviceApril 7, 2021· Bard Access Systems Inc.

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.

Class II — Potential Health HazardOngoing
Medical DeviceApril 6, 2021· Philips Respironics, Inc.

Recalled Item: BiPAP A40 System Silver Recalled by Philips Respironics, Inc. Due to Certain...

The Issue: Certain devices were built with motor assemblies that could contain...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 6, 2021· Philips Respironics, Inc.

Recalled Item: BiPAP A30 Recalled by Philips Respironics, Inc. Due to Certain devices were...

The Issue: Certain devices were built with motor assemblies that could contain...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 6, 2021· Philips Respironics, Inc.

Recalled Item: BiPAP A40 System Silver Recalled by Philips Respironics, Inc. Due to Certain...

The Issue: Certain devices were built with motor assemblies that could contain...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 6, 2021· Philips Respironics, Inc.

Recalled Item: BiPAP A40 Recalled by Philips Respironics, Inc. Due to Certain devices were...

The Issue: Certain devices were built with motor assemblies that could contain...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 6, 2021· Philips Respironics, Inc.

Recalled Item: BiPAP A40 Recalled by Philips Respironics, Inc. Due to Certain devices were...

The Issue: Certain devices were built with motor assemblies that could contain...

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

Class II — Potential Health HazardOngoing