Recall Recall Details
Endurant, Endurant II and Endurant IIs Stent Graft System: Medtronic Endurant Stent G ...
Endurant, Endurant II and Endurant IIs Stent Graft System:
Medtronic Endurant Stent Graft System Model/REF
ENBF2313C120EE;
ENBF2313C120EE;
ENBF2313C145EE;
ENBF2313C170EE;
ENBF2316C120EE;
ENBF2316C145EE;
ENBF2316C170EE;
ENBF2513C120EE;
ENBF2513C145EE;
ENBF2513C170EE;
ENBF2516C120EE;
ENBF2516C145EE;
ENBF2516C170EE;
ENBF2813C145EE;
ENBF2813C170EE;
ENBF2816C120EE;
ENBF2816C145EE;
ENBF2816C170EE;
ENBF3216C120EE;
ENBF3216C145EE;
ENBF3216C170EE;
ENBF3616C145EE;
ENBF3616C170EE;
ENCF2323C45EE;
ENCF2525C45EE;
ENCF2828C45EE;
ENCF3232C45EE;
ENCF3636C45EE;
ENTF2323C70EE;
ENTF2525C70EE;
ENTF2828C70EE;
Medtronic Endurant II Stent Graft System Model/REF
ETBF2313C124E;
ETBF2313C124EE;
ETBF2313C145EE;
ETBF2313C145EJ;
ETBF2313C166EE;
ETBF2313C166EJ;
ETBF2316C124E;
ETBF2316C124EE;
ETBF2316C124EJ;
ETBF2316C145E;
ETBF2316C145EE;
ETBF2316C145EJ;
ETBF2316C166E;
ETBF2316C166EE;
ETBF2316C166EJ;
ETBF2513C124E;
ETBF2513C124EE;
ETBF2513C124EJ;
ETBF2513C145EE;
ETBF2513C145EJ;
ETBF2513C166E;
ETBF2513C166EE;
ETBF2513C166EJ;
ETBF2516C124EE;
ETBF2516C145E;
ETBF2516C145EE;
ETBF2516C145EJ;
ETBF2516C166E;
ETBF2516C166EE;
ETBF2516C166EJ;
ETBF2813C124EE;
ETBF2813C124EJ;
ETBF2813C145E;
ETBF2813C145EE;
ETBF2813C145EJ;
ETBF2813C166E;
ETBF2813C166EE;
ETBF2813C166EJ;
ETBF2816C124EE;
ETBF2816C124EJ;
ETBF2816C145E;
ETBF2816C145EE;
ETBF2816C145EJ;
ETBF2816C166E;
ETBF2816C166EE;
ETBF2816C166EJ;
ETBF2820C124EE;
ETBF2820C145EE;
ETBF2820C145EJ;
ETBF2820C166E;
ETBF2820C166EE;
ETBF2820C166EJ;
ETBF3216C124E;
ETBF3216C124EE;
ETBF3216C124EJ;
ETBF3216C145E;
ETBF3216C145EE;
ETBF3216C145EJ;
ETBF3216C166EE;
ETBF3216C166EJ;
ETBF3220C124EE;
ETBF3220C145EE;
ETBF3220C166E;
ETBF3220C166EE;
ETBF3220C166EJ;
ETBF3616C145E;
ETBF3616C145EE;
ETBF3616C145EJ;
ETBF3616C166E;
ETBF3616C166EE;
ETBF3616C166EJ;
ETBF3620C145EE;
ETBF3620C166EE;
ETBF3620C166EJ;
ETCF2323C49E;
ETCF2323C49EE;
ETCF2525C49E;
ETCF2525C49EE;
ETCF2525C49EJ;
ETCF2828C49E;
ETCF2828C49EE;
ETCF2828C49EJ;
ETCF3232C49E;
ETCF3232C49EE;
ETCF3232C49EJ;
ETCF3636C49E;
ETCF3636C49EE;
ETCF3636C49EJ;
ETTF2323C70E;
ETTF2323C70EE;
ETTF2323C70EJ;
ETTF2525C70E;
ETTF2525C70EE;
ETTF2525C70EJ;
ETTF2828C70E;
ETTF2828C70EE;
ETTF2828C70EJ;
ETTF3232C70E;
ETTF3232C70EE;
ETTF3232C70EJ;
ETTF3636C70E;
ETTF3636C70EE;
ETTF3636C70EJ;
ETUF2314C102E;
ETUF2314C102EE;
ETUF2314C102EJ;
ETUF2514C102E;
ETUF2514C102EE;
ETUF2514C102EJ;
ETUF2814C102E;
ETUF2814C102EE;
ETUF2814C102EJ;
ETUF3214C102E;
ETUF3214C102EE;
ETUF3614C102E;
ETUF3614C102EE;
Medtronic Endurant IIs Stent Graft System Model/REF:
ESBF2314C103E;
ESBF2314C103EE;
ESBF2314C103EJ;
ESBF2514C103E;
ESBF2514C103EE;
ESBF2514C103EJ;
ESBF2814C103E;
ESBF2814C103EE;
ESBF2814C103EJ;
ESBF3214C103E;
ESBF3214C103EE;
ESBF3214C103EJ;
ESBF3614C103E;
ESBF3614C103EE;
ESBF3614C103EJ;
Used to treat infrarenal abdominal aortic or aortoiliac aneurysms using an endovascular approach.
Components:
Recall Date: Dec 21, 2021
Mfg:
Medtronic Vascular, Inc.
Mfg Country:
United States
Recall ID: 89387
Product ID: 191464
Enforcement Date: Mar 2, 2022
Last Published: Feb 18, 2022
__________
RecallMe Number: Z-0657-2022
RecallMe Status: Notified
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