AFX BA25-90/I20-30

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a company representative,health report with the FDA on 2020-03-31 for AFX BA25-90/I20-30 manufactured by Endologix.

Event Text Entries

[188549098] The device involved in the 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 afx with strata?.
Patient Sequence No: 1, Text Type: N, H10

[188549099] The patient was initially implanted with a bifurcated stent graft and a suprarenal stent graft extension to treat an abdominal aortic aneurysm. Approximately 6 years post initial procedure a follow-up computed tomography angiogram has revealed a possible type 3b endoleak. Patient is pending re-intervention.
Patient Sequence No: 1, Text Type: D, B5

MAUDE Entry Details

Report Number2031527-2020-00120
MDR Report Key9908804
Date Received2020-03-31
Date of Report2020-03-03
Date of Event2020-03-03
Date Mfgr Received2020-03-03
Device Manufacturer Date2013-07-29
Date Added to Maude2020-03-31
Event Key0
Report Source CodeManufacturer report
Manufacturer LinkY
Number of Patients in Event0
Adverse Event Flag3
Product Problem Flag3
Reprocessed and Reused Flag3
Health Professional3
Initial Report to FDA3
Report to FDA3
Event Location3
Manufacturer ContactMR. EMILE PINSONNEAULT
Manufacturer Street2 MUSICK ,
Manufacturer CityIRVINE CA 92618
Manufacturer CountryUS
Manufacturer Postal92618
Manufacturer Phone8009832284
Manufacturer G1ENDOLOGIX
Manufacturer Street2 MUSICK ,
Manufacturer CityIRVINE CA 92618
Manufacturer CountryUS
Manufacturer Postal Code92618
Single Use3
Remedial ActionRC
Previous Use Code3
Removal Correction NumberZ-0006-2019
Event Type3
Type of Report3

Device Details

Brand NameAFX
Product CodeMIH
Date Received2020-03-31
Model NumberBA25-90/I20-30
Lot Number1100966-042
Device Expiration Date2014-06-30
Device AvailabilityN
Device Eval'ed by MfgrR
Device Sequence No1
Device Event Key0
Manufacturer Address2 MUSICK , IRVINE CA 92618 US 92618


Patient NumberTreatmentOutcomeDate
101. Other 2020-03-31

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