FDA Adverse Event Injury Summary report: N

GUIDANT CORP

MDR report key: 789831 · Received November 16, 2006

Report

Report Number
789831
Event Type
Injury
Date Received
November 16, 2006
Date of Event
April 19, 2006
Report Date
November 9, 2006
Manufacturer
GUIDANT CORP
Product Code
LWS
Adverse Event
Yes
Report Source
User Facility report
Reporter Location
HI, US
Reporter Occupation
RISK MANAGER

Narratives

Description of Event or Problem · 1

ICD DISCHARGE.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1 GUIDANT CORP ICD GENERATOR LWS GUIDANT CORP H179 NA
2 GUIDANT CORP ICD GENERATOR LWS GUIDANT CORP 6744 NA

Patients

Seq Age Sex Outcome Treatment
1 78 YR Required Intervention