MAUDE Adverse Event Report: ENDOLOGIX AFX2; BIFURCATED STENT GRAFT

Model Number BEA28-90/I20-30

Device Problem Material Puncture/Hole (1504)

Patient Problem Aneurysm (1708)

Event Date 03/13/2024

Event Type  Injury  

Manufacturer Narrative

The device involved in this event will not be returned for evaluation as it remains implanted in the patient.Patient medical records and imaging studies will be requested for further evaluation by the clinical specialist.If additional information pertinent to the incident is obtained, a follow-up report will be submitted.Device iteration is afx2 h3 other text : device remains implanted.

Event Description

The patient underwent an endovascular aneurysm repair (evar) on (b)(6) 2022 with the implant of an afx2 bifurcated stent graft, an afx vela suprarenal, two (2)excluder legs, and a liminexx stent.This initial procedure is outside of the indications of use (off-label) due to the use of adjunctive devices not compatible with the afx2 system.Approximately one year post initial procedure the aneurysm had grown from 51mm to 56mm.Approximately 1.5 years post initial procedure, during a routine follow-up with computed tomography (ct) and intraoperative angiography, the aneurysm measured 62mm which the physician suspects is due to a type iiib endoleak.Reintervention is scheduled to be on (b)(6) 2024.

• Brand Name: AFX2
• Type of Device: BIFURCATED STENT GRAFT
• Manufacturer (Section D): ENDOLOGIX; 2 musick; irvine CA 92618
• Manufacturer (Section G): ENDOLOGIX; 2 musick; ,; irvine CA 92618
• Manufacturer Contact: gary kirchgater ; 2 musick; ,; irvine, CA 92618 ; 8009832284
• MDR Report Key: 19035163
• MDR Text Key: 339279993
• Report Number: 3011063223-2024-00043
• Device Sequence Number: 1
• Product Code: MIH
• UDI-Device Identifier: 00818009014559
• UDI-Public: (01)00818009014559(17)250315
• Combination Product (y/n): N
• Reporter Country Code: JA
• PMA/PMN Number: P040002
• Number of Events Reported: 1
• Summary Report (Y/N): N
• Report Source: Manufacturer
• Source Type: Other,Foreign,Health Professional,Distributor
• Reporter Occupation: Physician
• Remedial Action: Other
• Type of Report: Initial
• Report Date: 03/14/2024

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?: No
• Device Operator: Health Professional
• Device Model Number: BEA28-90/I20-30
• Device Lot Number: 2558258007
• Was Device Available for Evaluation?: No
• Is the Reporter a Health Professional?: Yes
• Initial Date Manufacturer Received: 03/14/2024
• Initial Date FDA Received: 04/03/2024
• Was Device Evaluated by Manufacturer?: Device Not Returned to Manufacturer
• Date Device Manufactured: 04/12/2022
• Is the Device Single Use?: Yes
• Is This a Reprocessed and Reused Single-Use Device?: No
• Type of Device Usage: Initial
• Removal/Correction Number: Z-0007-2019
• Patient Sequence Number: 1
• Treatment: AFX VELA SUPRARENAL, LOT # 2556692011; EXCLUDER LEG (NON-ENDOLOGIX) LN UNK; EXCLUDER LEG (NON-ENDOLOGIX) LN UNK; LIMINEXX STENT (NON-ENDOLOGIX) LN UNK
• Patient Outcome(s): Other
• Patient Age: 81 YR
• Patient Sex: Male