Product Recalls in Montana

Product recalls affecting Montana — including food, drugs, consumer products, medical devices, and vehicles distributed to Montana. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 1,073 recalls have been distributed to Montana in the last 12 months.

48,326 total recalls
1,073 in last 12 months

Showing 5561–5580 of 48,326 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· 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
Medical DeviceMay 3, 2024· Philips North America Llc

Recalled Item: MR RT - Magnetic Resonance (MR) systems are Medical Electrical 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· 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 TX for PET Model Number (REF): 781479 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 Elition 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· 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: HA FlexTrak II-Patient transport functionality to transport the patient from...

The Issue: Oil may leak from the HA FlexTrack Trolley onto the floor when pressing 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: 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.

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

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.

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· Philips North America Llc

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.

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

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.

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: 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.

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

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.

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

Recalled Item: Achieva 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: Panorama HFO- 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