Product Recalls in Mississippi

Product recalls affecting Mississippi — including food, drugs, consumer products, medical devices, and vehicles distributed to Mississippi. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 2,645 recalls have been distributed to Mississippi in the last 12 months.

49,744 total recalls
2,645 in last 12 months

Showing 40014020 of 28,172 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: 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
Medical DeviceMay 3, 2024· Philips North America Llc

Recalled Item: Ingenia Ambition S Model Number (REF): (1) 782139 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: Ingenia Ambition X- 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.

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

Recalled Item: SmartPath to dStream for 3.0T Model Number (REF): 782145 Recalled by Philips...

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: Evolution upgrade 3.0T Model Number (REF): (1)782117 Recalled by Philips...

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: Evolution upgrade 1.5T- 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.

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

Recalled Item: MR 5300- 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.

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

Recalled Item: MR RT Upgrades- 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.

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

Recalled Item: Sonalleve MR HIFU 3.0T - Magnetic Resonance (MR) systems are 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.

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

Recalled Item: Intera 1.5T- 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.

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

Recalled Item: Achieva 1.5T Initial system Model Number (REF): 781178 Recalled by Philips...

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