FDA Adverse Event Injury Summary report: N

GDC-10 360 COIL

MDR report key: 1211747 · Received October 24, 2008

Report

Report Number
2939204-2008-00503
Event Type
Injury
Date Received
October 24, 2008
Date of Event
January 15, 2008
Report Date
October 6, 2008
Manufacturer
NEUROVASCULAR DIVISION, BOSTON SCIENTIFIC CORP.
Product Code
HCG
PMA / PMN Number
K042539
Adverse Event
Yes
Report Source
Manufacturer report
Reporter Location
TX, US
Reporter Occupation
PHYSICIAN

Narratives

Additional Manufacturer Narrative · 1

TRANSIENT HAND DISCOORDINATION. NO ALLEGATION OF PRODUCT MALFUNCTION OR NON CONFORMANCE CONTRIBUTING TO THE REPORTED EVENT.

Description of Event or Problem · 1

THE PT UNDER WENT THE SUCCESSFUL STENT ASSISTED EMBOLIZATION OF RIGHT PARACLINOID/OPHTHALMIC ARTERY ANEURYSM. ONE MONTH POST PROCEDURE, THE PT PRESENTED WITH TRANSIENT HAND DISCOORDINATION "POSSIBLY DUE TO A SMALL EMBOLIC EVENT." THE PT WAS TREATED WITH ASPIRIN THERAPY THAT THE PT HAD PREVIOUSLY STOPPED. TWO MONTHS LATER, IT WAS REPORTED THAT THE DISCOORDINATION WAS RESOLVED WITHOUT ANY RESIDUAL EFFECTS.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1 GDC-10 360 COIL (HCG) DEATACHABLE COIL HCG NEUROVASCULAR DIVISION, BOSTON SCIENTIFIC CORP. 346407-SR 9450579

Patients

Seq Age Sex Outcome Treatment
1 66 YR Required Intervention SIX BOSTON SCIENTIFIC GDC COILS