Product Recalls in Delaware

Product recalls affecting Delaware — including food, drugs, consumer products, medical devices, and vehicles distributed to Delaware. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 2,020 recalls have been distributed to Delaware in the last 12 months.

48,330 total recalls
2,020 in last 12 months

Showing 39613980 of 27,373 recalls

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· 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· 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: 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 1.5T CX - Magnetic Resonance (MR) systems are Medical 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· 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: 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· 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: 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