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. 2,832 recalls have been distributed to Virginia in the last 12 months.

53,829 total recalls
2,832 in last 12 months

Showing 40414060 of 29,425 recalls

Medical DeviceMay 3, 2024· Atrium Medical Corporation

Recalled Item: ADVANTA VXT Recalled by Atrium Medical Corporation Due to Complaints of...

The Issue: Complaints of reported separation of the Slider GDS Swivel Rod from the...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 3, 2024· Atrium Medical Corporation

Recalled Item: FLIXENE Recalled by Atrium Medical Corporation Due to Complaints of reported...

The Issue: Complaints of reported separation of the Slider GDS Swivel Rod from the...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 3, 2024· Atrium Medical Corporation

Recalled Item: ADVANTA VXT Recalled by Atrium Medical Corporation Due to Complaints of...

The Issue: Complaints of reported separation of the Slider GDS Swivel Rod from the...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 3, 2024· Atrium Medical Corporation

Recalled Item: ADVANTA VXT Recalled by Atrium Medical Corporation Due to Complaints of...

The Issue: Complaints of reported separation of the Slider GDS Swivel Rod from the...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 3, 2024· Atrium Medical Corporation

Recalled Item: ADVANTA VXT Recalled by Atrium Medical Corporation Due to Complaints of...

The Issue: Complaints of reported separation of the Slider GDS Swivel Rod from the...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 3, 2024· Atrium Medical Corporation

Recalled Item: ADVANTA VXT Recalled by Atrium Medical Corporation Due to Complaints of...

The Issue: Complaints of reported separation of the Slider GDS Swivel Rod from the...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 3, 2024· Atrium Medical Corporation

Recalled Item: FLIXENE Recalled by Atrium Medical Corporation Due to Complaints of reported...

The Issue: Complaints of reported separation of the Slider GDS Swivel Rod from the...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 3, 2024· Atrium Medical Corporation

Recalled Item: FLIXENE Recalled by Atrium Medical Corporation Due to Complaints of reported...

The Issue: Complaints of reported separation of the Slider GDS Swivel Rod from the...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 3, 2024· Atrium Medical Corporation

Recalled Item: ADVANTA VXT Recalled by Atrium Medical Corporation Due to Complaints of...

The Issue: Complaints of reported separation of the Slider GDS Swivel Rod from the...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 3, 2024· Atrium Medical Corporation

Recalled Item: ADVANTA VXT Recalled by Atrium Medical Corporation Due to Complaints of...

The Issue: Complaints of reported separation of the Slider GDS Swivel Rod from the...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 3, 2024· Atrium Medical Corporation

Recalled Item: ADVANTA VXT Recalled by Atrium Medical Corporation Due to Complaints of...

The Issue: Complaints of reported separation of the Slider GDS Swivel Rod from the...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 3, 2024· Atrium Medical Corporation

Recalled Item: ADVANTA VXT Recalled by Atrium Medical Corporation Due to Complaints of...

The Issue: Complaints of reported separation of the Slider GDS Swivel Rod from the...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 3, 2024· Atrium Medical Corporation

Recalled Item: ADVANTA VXT Recalled by Atrium Medical Corporation Due to Complaints of...

The Issue: Complaints of reported separation of the Slider GDS Swivel Rod from the...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 3, 2024· Atrium Medical Corporation

Recalled Item: ADVANTA VXT Recalled by Atrium Medical Corporation Due to Complaints of...

The Issue: Complaints of reported separation of the Slider GDS Swivel Rod from the...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 3, 2024· Atrium Medical Corporation

Recalled Item: ADVANTA VXT Recalled by Atrium Medical Corporation Due to Complaints of...

The Issue: Complaints of reported separation of the Slider GDS Swivel Rod from the...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 3, 2024· Atrium Medical Corporation

Recalled Item: ADVANTA VXT Recalled by Atrium Medical Corporation Due to Complaints of...

The Issue: Complaints of reported separation of the Slider GDS Swivel Rod from the...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 3, 2024· Atrium Medical Corporation

Recalled Item: ADVANTA VXT Recalled by Atrium Medical Corporation Due to Complaints of...

The Issue: Complaints of reported separation of the Slider GDS Swivel Rod from the...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 3, 2024· Atrium Medical Corporation

Recalled Item: ADVANTA VXT Recalled by Atrium Medical Corporation Due to Complaints of...

The Issue: Complaints of reported separation of the Slider GDS Swivel Rod from the...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 3, 2024· Philips North America Llc

Recalled Item: Achieva 3.0T Model Number (REF): (1) 781345 Recalled by Philips North...

The Issue: The g-MDU (global Mains Distribution Unit) L3 terminal connection may become...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 3, 2024· Philips North America Llc

Recalled Item: MR system 1.5T Marlin- Magnetic Resonance (MR) systems are Medical Recalled...

The Issue: The g-MDU (global Mains Distribution Unit) L3 terminal connection may become...

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

Class II — Potential Health HazardOngoing