Endurant™ / Endurant II ™ 23mm and 25mm Bifurcated Stent Graft Systems
Model / Serial
Affected Endurant / Endurant II Model Numbers: ENBF2313C120EE, ETBF2313C166EE, ENBF2313C145EE, ETBF2316C124EE, ENBF2313C170EE, ETBF2316C145EE, ENBF2316C145EE, ETBF2316C166E, ENBF2316C170EE, ETBF2316C166EE, ENBF2513C145EE, ETBF2513C124EE, ENBF2513C170EE, ETBF2513C145EE, ENBF2516C145EE, ETBF2513C166EE, ENBF2516C170EE, ETBF2516C124EE, ETBF2313C124E, ETBF2516C145E, ETBF2313C124EE, ETBF2516C145EE, ETBF2313C145EE, ETBF2516C166E, ETBF2313C166E, ETBF2516C166EE
Note: Only specific serial numbers are affected, please use the website link provided in the attached FSN to determine whether a serial number is affected or not.
“If our surveillance systems identify a potential performance issue, our personnel promptly evaluate the problem, including, when appropriate, conducting root cause investigations and internal testing to assess whether the product continues to meet specifications and defined performance criteria,” Medtronic told ICIJ in a statement. “In some cases, based on this evaluation, Medtronic may determine that a recall is necessary.” The company said that it communicates with healthcare providers and/or patients and provide recommendations to address such issues. Medtronic noted that these communications can include letters, emails, calls, press releases, physician notifications and social media postings, as well as informing the FDA and other regulators of the actions.