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Atrium Medical Recalls
150 recalls on record · August 21, 2013 to October 16, 2024 · Medical Devices
Recalls by year
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Count of recall notices naming this brand, by the year the recall was announced. A quiet year is not proof of a safe year.
October 16, 2024Medical DevicesFDA
Atrium Medical Corporation recalls iCast Covered Stent, 6MMx16MMx120CM, Model Number 42616
Hazard: There is an error in the Unique Device Identifier (UDI) printed on the product's distribution label.
June 12, 2024Medical DevicesFDA
Atrium Medical Corporation recalls FLIXENE, 4-7X30, 2GDS, GWT-GW. Double-Ended Slider GDS. Vascular graft
Hazard: Complaints of reported separation of the Slider GDS Swivel Rod from the Swivel Core and of a notable gap between the two pieces.
June 12, 2024Medical DevicesFDA
Atrium Medical Corporation recalls FLIXENE, 4-7X45, 2GDS, GWT-GW. Double-Ended Slider GDS. Vascular graft
Hazard: Complaints of reported separation of the Slider GDS Swivel Rod from the Swivel Core and of a notable gap between the two pieces.
June 12, 2024Medical DevicesFDA
Atrium Medical Corporation recalls FLIXENE, 4-6X45, 2GDS, GWT-GW. Double-Ended Slider GDS. Vascular graft
Hazard: Complaints of reported separation of the Slider GDS Swivel Rod from the Swivel Core and of a notable gap between the two pieces.
June 12, 2024Medical DevicesFDA
Atrium Medical Corporation recalls FLIXENE, 4-7X45, 2GDS, GWT. Double-Ended Slider GDS. Vascular graft
Hazard: Complaints of reported separation of the Slider GDS Swivel Rod from the Swivel Core and of a notable gap between the two pieces.
June 12, 2024Medical DevicesFDA
Atrium Medical Corporation recalls FLIXENE, 4-6X45, 2GDS, GWT. Double-Ended Slider GDS. Vascular graft
Hazard: Complaints of reported separation of the Slider GDS Swivel Rod from the Swivel Core and of a notable gap between the two pieces.
June 12, 2024Medical DevicesFDA
Atrium Medical Corporation recalls FLIXENE, 4-7X35, 2GDS, GWT-GW. Double-Ended Slider GDS. Vascular graft
Hazard: Complaints of reported separation of the Slider GDS Swivel Rod from the Swivel Core and of a notable gap between the two pieces.
June 12, 2024Medical DevicesFDA
Atrium Medical Corporation recalls FLIXENE, 4-6X35, 2GDS, GWT-GW. Double-Ended Slider GDS. Vascular graft
Hazard: Complaints of reported separation of the Slider GDS Swivel Rod from the Swivel Core and of a notable gap between the two pieces.
June 12, 2024Medical DevicesFDA
Atrium Medical Corporation recalls FLIXENE, 6X30, 1GDS, STR. Single-Ended Slider GDS. Vascular graft
Hazard: Complaints of reported separation of the Slider GDS Swivel Rod from the Swivel Core and of a notable gap between the two pieces.
June 12, 2024Medical DevicesFDA
Atrium Medical Corporation recalls FLIXENE, 7X50, 1GDS, STR. Single-Ended Slider GDS. Vascular graft
Hazard: Complaints of reported separation of the Slider GDS Swivel Rod from the Swivel Core and of a notable gap between the two pieces.
June 12, 2024Medical DevicesFDA
Atrium Medical Corporation recalls FLIXENE, 6X50, 1GDS, STR. Single-Ended Slider GDS. Vascular graft
Hazard: Complaints of reported separation of the Slider GDS Swivel Rod from the Swivel Core and of a notable gap between the two pieces.
June 12, 2024Medical DevicesFDA
Atrium Medical Corporation recalls FLIXENE, 7X30, 1GDS, GW. Single-Ended Slider GDS. Vascular graft
Hazard: Complaints of reported separation of the Slider GDS Swivel Rod from the Swivel Core and of a notable gap between the two pieces.
June 12, 2024Medical DevicesFDA
Atrium Medical Corporation recalls FLIXENE, 6X30, 1GDS, GW. Single-Ended Slider GDS. Vascular graft
Hazard: Complaints of reported separation of the Slider GDS Swivel Rod from the Swivel Core and of a notable gap between the two pieces.
June 12, 2024Medical DevicesFDA
Atrium Medical Corporation recalls FLIXENE, 7X80, 1GDS, GW. Single-Ended Slider GDS. Vascular graft
Hazard: Complaints of reported separation of the Slider GDS Swivel Rod from the Swivel Core and of a notable gap between the two pieces.
June 12, 2024Medical DevicesFDA
Atrium Medical Corporation recalls FLIXENE, 7X40, 1GDS, GW. Single-Ended Slider GDS. Vascular graft
Hazard: Complaints of reported separation of the Slider GDS Swivel Rod from the Swivel Core and of a notable gap between the two pieces.
June 12, 2024Medical DevicesFDA
Atrium Medical Corporation recalls FLIXENE, 6X40, 1GDS, GW. Single-Ended Slider GDS. Vascular graft
Hazard: Complaints of reported separation of the Slider GDS Swivel Rod from the Swivel Core and of a notable gap between the two pieces.
June 12, 2024Medical DevicesFDA
Atrium Medical Corporation recalls FLIXENE, 7X50, 1GDS, GW. Single-Ended Slider GDS. Vascular graft
Hazard: Complaints of reported separation of the Slider GDS Swivel Rod from the Swivel Core and of a notable gap between the two pieces.
June 12, 2024Medical DevicesFDA
Atrium Medical Corporation recalls FLIXENE, 6X50, 1GDS, GW. Single-Ended Slider GDS. Vascular graft
Hazard: Complaints of reported separation of the Slider GDS Swivel Rod from the Swivel Core and of a notable gap between the two pieces.
June 12, 2024Medical DevicesFDA
Atrium Medical Corporation recalls ADVANTA VXT, 5-8X80, 1GDS, FH, TPR-TW. Single-Ended Slider GDS. Vascular graft
Hazard: Complaints of reported separation of the Slider GDS Swivel Rod from the Swivel Core and of a notable gap between the two pieces.
June 12, 2024Medical DevicesFDA
Atrium Medical Corporation recalls ADVANTA VXT, 4-7X80, 1GDS, FH, TPR-TW. Single-Ended Slider GDS. Vascular graft
Hazard: Complaints of reported separation of the Slider GDS Swivel Rod from the Swivel Core and of a notable gap between the two pieces.
June 12, 2024Medical DevicesFDA
Atrium Medical Corporation recalls ADVANTA VXT, 4-7X45, 1GDS, CH, TPR-SW. Single-Ended Slider GDS. Vascular graft
Hazard: Complaints of reported separation of the Slider GDS Swivel Rod from the Swivel Core and of a notable gap between the two pieces.
June 12, 2024Medical DevicesFDA
Atrium Medical Corporation recalls ADVANTA VXT, 4-6X45, 1GDS, CH, TPR-SW. Single-Ended Slider GDS. Vascular graft
Hazard: Complaints of reported separation of the Slider GDS Swivel Rod from the Swivel Core and of a notable gap between the two pieces.
June 12, 2024Medical DevicesFDA
Atrium Medical Corporation recalls ADVANTA VXT, 4-7X45, 2GDS, NH, TPR-SW. Single-Ended Slider GDS. Vascular graft
Hazard: Complaints of reported separation of the Slider GDS Swivel Rod from the Swivel Core and of a notable gap between the two pieces.
June 12, 2024Medical DevicesFDA
Atrium Medical Corporation recalls ADVANTA VXT, 4-7X70, 1GDS, NH, TPR-SW. Single-Ended Slider GDS. Vascular graft
Hazard: Complaints of reported separation of the Slider GDS Swivel Rod from the Swivel Core and of a notable gap between the two pieces.
June 12, 2024Medical DevicesFDA
Atrium Medical Corporation recalls ADVANTA VXT, 5-8X45, 1GDS, NH, TPR-SW. Single-Ended Slider GDS. Vascular graft
Hazard: Complaints of reported separation of the Slider GDS Swivel Rod from the Swivel Core and of a notable gap between the two pieces.
June 12, 2024Medical DevicesFDA
Atrium Medical Corporation recalls ADVANTA VXT, 4-7X45, 1GDS, NH, TPR-SW. Single-Ended Slider GDS. Vascular graft
Hazard: Complaints of reported separation of the Slider GDS Swivel Rod from the Swivel Core and of a notable gap between the two pieces.
June 12, 2024Medical DevicesFDA
Atrium Medical Corporation recalls ADVANTA VXT, 4-6X45, 1GDS, NH, TPR-SW. Single-Ended Slider GDS. Vascular graft
Hazard: Complaints of reported separation of the Slider GDS Swivel Rod from the Swivel Core and of a notable gap between the two pieces.
June 12, 2024Medical DevicesFDA
Atrium Medical Corporation recalls ADVANTA VXT, 6X45, 1GDS, CH, STR-SW. Single-Ended Slider GDS. Vascular graft
Hazard: Complaints of reported separation of the Slider GDS Swivel Rod from the Swivel Core and of a notable gap between the two pieces.
June 12, 2024Medical DevicesFDA
Atrium Medical Corporation recalls ADVANTA VXT, 6X100, 1GDS, FH, STR-TW. Single-Ended Slider GDS. Vascular graft
Hazard: Complaints of reported separation of the Slider GDS Swivel Rod from the Swivel Core and of a notable gap between the two pieces.
June 12, 2024Medical DevicesFDA
Atrium Medical Corporation recalls ADVANTA VXT, 8X80, 1GDS, FH, STR-TW. Single-Ended Slider GDS. Vascular graft
Hazard: Complaints of reported separation of the Slider GDS Swivel Rod from the Swivel Core and of a notable gap between the two pieces.