FDA Adverse Event Death Summary report: N

V 2.5 SOFT EXT

MDR report key: 3276608 · Received August 9, 2013

Report

Report Number
0002954917-2013-00109
Event Type
Death
Date Received
August 9, 2013
Date of Event
February 7, 2013
Report Date
July 26, 2013
Manufacturer
CONCENTRIC MEDICAL
Product Code
NRY
PMA / PMN Number
K090085
Adverse Event
Yes
Report Source
Manufacturer report
Reporter Location
JA
Reporter Occupation
PHYSICIAN

Narratives

Additional Manufacturer Narrative · 1

THE SUBJECT DEVICE IS NOT AVAILABLE FOR ANALYSIS; THEREFORE, ANALYSIS CANNOT BE PERFORMED. FROM THE INFORMATION AVAILABLE, THERE IS NO INDICATION THAT THE REPORTED EVENT IS RELATED TO PRODUCT SPECIFICATIONS NONCONFORMANCE OR MISUSE. THERE IS ALSO NO INDICATION THAT THE SUBJECT DEVICE MALFUNCTIONED. HOWEVER, HEMORRHAGE AND PATIENT OUTCOME OF DEATH ARE KNOWN RISKS ASSOCIATED WITH ENDOVASCULAR PROCEDURES AND ARE NOTED AS SUCH IN THE DIRECTIONS FOR USE (DFU). THEREFORE, A ROOT CAUSE OF ANTICIPATED PROCEDURAL COMPLICATIONS HAS BEEN ASSIGNED TO THIS EVENT.

Additional Manufacturer Narrative · 1

SUBJECT DEVICE IS NOT AVAILABLE.

Description of Event or Problem · 1

IT WAS REPORTED THAT POST THROMBECTOMY OF THE OCCLUDED BASILAR ARTERY A SUBARACHNOID HEMORRHAGE OCCURRED (SAH). THE PHYSICIAN ADMINISTERED 30MG OF TISSUE PLASMINOGEN ACTIVATOR (T-PA) INTRAVENOUSLY. THE PATIENT DIED FIVE DAYS POST PROCEDURE DUE TO THE SAH. NO ADDITIONAL INFORMATION IS AVAILABLE.

Description of Event or Problem · 1

IT WAS REPORTED THAT POST THROMBECTOMY OF THE OCCLUDED BASILAR ARTERY A SUBARACHNOID HEMORRHAGE OCCURRED (SAH). THE PHYSICIAN ADMINISTERED 30MG OF TISSUE PLASMINOGEN ACTIVATOR (T-PA) INTRAVENOUSLY. THE PATIENT DIED FIVE DAYS POST PROCEDURE DUE TO THE SAH. NO ADDITIONAL INFORMATION IS AVAILABLE.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
377356 V 2.5 SOFT EXT CATHETER, THROMBUS RETRIEVER NRY CONCENTRIC MEDICAL UNKNOWN

Patients

Seq Age Sex Outcome Treatment
1 69 YR Death| R