FDA Adverse Event Injury Summary report: N

TELECTRONICS 030-362

MDR report key: 65427 · Received January 24, 1997

Report

Report Number
1316542-1997-00132
Event Type
Injury
Date Received
January 24, 1997
Date of Event
August 1, 1996
Report Date
January 24, 1997
Manufacturer
TELECTRONICS PACING SYSTEMS
Product Code
DTB
Adverse Event
Yes
Report Source
Manufacturer report
Reporter Location
OH, US
Reporter Occupation
NURSE

Narratives

Description of Event or Problem · 1

LEAD WAS CUT AND CAPPED DUE TO A REPORT OF INSULATION SEPARATION AT PROXIMAL PIN. NO FURTHER INJURY OR COMPLICATIONS ASSOCIATED WITH THE EVENT.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1 TELECTRONICS 030-362 Implant PERMANENT IMPLANTABLE PACEMAKER ELECTRODE DTB TELECTRONICS PACING SYSTEMS 030-362 NA

Patients

Seq Age Sex Outcome Treatment
1 62 YR Required Intervention