FDA Adverse Event Injury Summary report: N

WINGSPAN STENT

MDR report key: 2063283 · Received April 19, 2011

Report

Report Number
2939204-2011-00219
Event Type
Injury
Date Received
April 19, 2011
Date of Event
March 16, 2011
Report Date
April 6, 2011
Manufacturer
BOSTON SCIENTIFIC - FREMONT
Product Code
NJE
PMA / PMN Number
H050001
Adverse Event
Yes
Report Source
Manufacturer report
Reporter Occupation
PHYSICIAN

Narratives

Additional Manufacturer Narrative · 1

(B)(4).

Additional Manufacturer Narrative · 1

THE DEVICE REMAINS IMPLANTED SO WAS NOT AVAILABLE FOR EVALUATION. FROM THE INFORMATION PROVIDED THERE IS NO INDICATION THAT THERE WAS ANY DEVICE MALFUNCTION, NONCONFORMANCE OR MISUSE THAT CONTRIBUTED TO THE REPORTED EVENT. STROKE IS A KNOWN AND ANTICIPATED COMPLICATION TO THESE TYPES OF PROCEDURES AND IS LISTED AS SUCH IN THE DIRECTIONS FOR USE. THEREFORE IT WAS DETERMINED THAT THE REPORTED EVENT WAS AN ANTICIPATED PROCEDURAL COMPLICATION.

Description of Event or Problem · 1

ONE DAY POST PROCEDURE THE PATIENT SUFFERED A MINOR STROKE WITH LACUNAR INFARCTION IN THE RIGHT CEREBELLAR HEMISPHERE AND IN THE VERMIS CEREBELLI IN THE TERRITORY OF THE TREATED VESSEL (BASILAR ARTERY). THE STROKE RESOLVED WITH RESIDUAL SEQUELAE OF LATENT RIGHT HEMIPARESIS AND A LIMPING GAIT.

Description of Event or Problem · 1

ONE DAY POST PROCEDURE THE PATIENT SUFFERED A MINOR STROKE WITH LACUNAR INFARCTION IN THE RIGHT CEREBELLAR HEMISPHERE AND IN THE VERMIS CEREBELLI IN THE TERRITORY OF THE TREATED VESSEL (BASILAR ARTERY). THE STROKE RESOLVED WITH RESIDUAL SEQUELAE OF LATENT RIGHT HEMIPARESIS AND A LIMPING GAIT.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1 WINGSPAN STENT STENT, INTRACRANIAL NEUROVASCULAR NJE BOSTON SCIENTIFIC - FREMONT M003WE0350200

Patients

Seq Age Sex Outcome Treatment
1 76 YR Other GATEWAY BALLOON (BOSTON SCIENTIFIC)