MAUDE Adverse Event Report: MEDTRONIC IRELAND VALIANT CAPTIVIA - FF; SYSTEM, ENDOVASCULAR GRAFT, AORTIC ANEURYSM TREATMENT

Model Number	VAMF3232C200TU
Medical Device Problem Code	Device Damaged by Another Device (2915)
Health Effect - Clinical Codes	No Consequences Or Impact To Patient (2199); Injury (2348)
Date of Event	02/24/2020
Type of Reportable Event	Serious Injury
Additional Manufacturer Narrative
If information is provided in the future, a supplemental report will be issued.
Event or Problem Description
Two valiant captivia stent grafts were implanted in the endovascular treatment of a 57mm thoracic aortic aneurysm.It was reported that when the patient returned for follow-up 3 years and 3 months later, a ct was performed where contrast in the sac was present.Initially it was unclear whether it was a type ii or type iii endoleak.A diagnostic angiogram was performed on the same date and the endoleak was confirmed to be a type iiib graft defect.As per the physician it was believed that the bare stent of the 32mm distal component has eroded through the fabric of the 36mm proximal component.There was no change in aneurysm sac diameter since initial implant.As per the physician the cause of the event was friction.No additional clinical sequalae were provided and the patient will be monitored.
Additional Manufacturer Narrative
Additional information: a secondary procedure was carried out and the existing devices were relined with a 37 x 37 x 1 82 navion coverseal which was done without incident landing distal to the left subclavian artery and extending through the existing devices and covering the fabric defect.It was also reported that during the initial repair the 32mm valiant captivia was implanted distal with the bare stent apposed to the aortic wall.The 36mm valiant captivia was then used to extend to the left subclavian artery.All the bare stent was in contact with the aortic wall, not within a graft.Updated film evaluation summary: the reported type iiib endoleak could not be confirmed from the single still films provided and so the cause of the event could not be determined.Other than the calcification seen along the proximal seal zone, analysis of the returned pre-implant film report did not reveal any anatomical characteristics that could explain the reported endoleak.Images during implant and post-implant ct¿s were not provided for a complete assessment.Lack of additional angiography cine images showing the endoleak did not permit a more comprehensive analysis of the endoleak source/cause.Endoleak interrogation via selective angiograms (injecting from different levels within the stent graft) to help determine the source and rule out other potential endoleak sources was not seen, and only a single imaging view point (a-p) was observed in the films provided; thereby, making assessment of the endoleak difficult.It is possible that stent abrasion across the overlapping devices may have a led to a type iiib endoleak.Calcification seen along the length of the proximal seal zone from the pre-implant films may have also led to external fabric abrasion.It is unknown if disease progression or aneurysm morphology changes occurring after stent implantation may have been a contributor to the reported event.No stent graft issues were observed on the films received.If information is provided in the future, a supplemental report will be issued.

• Brand Name: VALIANT CAPTIVIA - FF
• Common Device Name: SYSTEM, ENDOVASCULAR GRAFT, AORTIC ANEURYSM TREATMENT
• Manufacturer (Section D): MEDTRONIC IRELAND; parkmore business park west; galway
• MDR Report Key: 9768576
• Report Number: 9612164-2020-00928
• Device Sequence Number: 16866623
• Product Code: MIH
• UDI-Device Identifier: 00643169347137
• UDI-Public: 00643169347137
• Combination Product (Y/N): N
• Initial Reporter State: WI
• Initial Reporter Country: US
• PMA/510(K) Number: P100040
• Number of Events Summarized: 1
• Summary Report (Y/N): N
• Device Implanted Year: 2016
• Reporter Type: Manufacturer
• Report Source: company representative,health
• Initial Reporter Occupation: Physician
• Type of Report: Initial,Followup
• Report Date (Section B): 04/02/2020

1 Device was Involved in the Event

1 Patient was Involved in the Event

• Is this an Adverse Event Report?: Yes
• Is this a Product Problem Report?: Yes
• Operator of Device: Health Professional
• Device Expiration Date: 04/08/2018
• Device Model Number: VAMF3232C200TU
• Device Catalogue Number: VAMF3232C200TU
• Was Device Available for Evaluation?: Device Returned to Manufacturer
• Date Returned to Manufacturer: 02/26/2020
• Initial Date Received by Manufacturer: 02/26/2020
• Supplement Date Received by Manufacturer: 03/11/2020
• Initial Report FDA Received Date: 02/28/2020
• Supplement Report FDA Received Date: 04/02/2020
• Is This a Single-Use Device that was Reprocessed and Reused on a Patient? (Y/N): No
• Patient Sequence Number: 1
• Outcome Attributed to Adverse Event: Required Intervention
• Patient Age: 84 YR