Product Recalls in Maryland

Product recalls affecting Maryland — including food, drugs, consumer products, medical devices, and vehicles distributed to Maryland. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 2,882 recalls have been distributed to Maryland in the last 12 months.

52,535 total recalls
2,882 in last 12 months

Showing 40014020 of 29,093 recalls

Medical DeviceMay 6, 2024· NovaSignal Corp.

Recalled Item: NovaGuide 2 Intelligent Ultrasound Recalled by NovaSignal Corp. Due to Due...

The Issue: Due to inadvertently disconnecting grounding cable of ultrasound system...

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: 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: 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· Philips North America Llc

Recalled Item: HA FlexTrak-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: 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: 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