AFX BA25-90/I16-30

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/I16-30 manufactured by Endologix.

MAUDE Entry Details

Report Number2031527-2020-00119
MDR Report Key9908775
Report SourceCOMPANY REPRESENTATIVE,HEALTH
Date Received2020-03-31
Date of Report2020-03-02
Date of Event2020-03-02
Date Mfgr Received2020-03-02
Device Manufacturer Date2011-12-06
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
Generic NameBIFURCATED STENT GRAFT
Product CodeMIH
Date Received2020-03-31
Model NumberBA25-90/I16-30
Lot NumberW11-5852-014
Device Expiration Date2012-10-31
OperatorHEALTH PROFESSIONAL
Device AvailabilityN
Device Eval'ed by MfgrR
Device Sequence No1
Device Event Key0
ManufacturerENDOLOGIX
Manufacturer Address2 MUSICK , IRVINE CA 92618 US 92618


Patients

Patient NumberTreatmentOutcomeDate
101. Other 2020-03-31

© 2020 FDA.report
This site is not affiliated with or endorsed by the FDA.