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. 2,134 recalls have been distributed to Virginia in the last 12 months.
Showing 4021–4040 of 29,425 recalls
Recalled Item: AchievaXR -Magnetic Resonance (MR) systems are Medical Electrical Systems...
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.
Recalled Item: Ingenia 1.5T S Model Number (REF): 781347 Recalled by Philips North America...
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.
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.
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.
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.
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.
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.
Recalled Item: SmartPath to Ingenia Elition X - Magnetic Resonance (MR) systems Recalled by...
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.
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.
Recalled Item: SmartPath to dStream for XR and 3.0T- Magnetic Resonance (MR) Recalled by...
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.
Recalled Item: Upgrade dStream - Magnetic Resonance (MR) systems are Medical Electrical...
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.
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.
Recalled Item: Achieva 1.5T Conversion- Magnetic Resonance (MR) systems are Medical...
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.
Recalled Item: SmartPath to dStream for 1.5T- Magnetic Resonance (MR) systems are 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.
Recalled Item: Ingenia 3.0T CX Model Number (REF): (1) 782105 (2) 781271 Recalled by...
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.
Recalled Item: Marlin 1.5T - Magnetic Resonance (MR) systems are Medical Electrical...
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.
Recalled Item: Achieva 3.0T for PET -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.
Recalled Item: Brand Name: Cerene Cryotherapy Device Product Name: DEVICE Recalled by...
The Issue: Error code 003 was not listed in certain rows of the Device Instructions for...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ingenia 3.0T- Magnetic Resonance (MR) systems are Medical Electrical Systems...
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.
Recalled Item: Ingenia 1.5T Model Number (REF): (1) 782140 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.