Adverse Events Associated with Mechanical Thrombectomy Devices in Peripheral Interventions: Review of the Manufacturer and User Facility Device Experience (MAUDE) Database

被引:1
作者
Ahmad, Yusuf [1 ]
Jacobsen, Torrin [1 ]
Anthony, Stefan [1 ]
Asad, Nafisa [1 ]
Ahmed, Osman [2 ]
机构
[1] Lake Erie Coll Osteopath Med, Erie, PA 16509 USA
[2] Univ Chicago, Dept Radiol, Sect Vasc & Intervent Radiol, Chicago, IL USA
关键词
D O I
10.1016/j.jvir.2024.03.019
中图分类号
R8 [特种医学]; R445 [影像诊断学];
学科分类号
1002 ; 100207 ; 1009 ;
摘要
引用
收藏
页数:6
相关论文
共 4 条
[1]  
Araujo ST, 2019, Cochrane Database Syst Rev, V2019
[2]  
MacKenzie IER, 2020, WORLD NEUROSURG, V138, pE839, DOI [10.1016/j.wneu.2020.03.105, 10.1016/J.WNEu.2020.03.105]
[3]  
U.S. Food and Drug Administration, 2022, Class 2 device recall Fogarty arterial embolectomy catheters and Fogarty biliary balloon probes
[4]  
U.S. Food and Drug Administration, 2015, Class 2 device recall AngioJet SOLENT Omni thrombectomy set