FDA Adverse Event Injury Summary report: N

TRIUMPH I PORT

MDR report key: 41635 · Received September 30, 1996

Report

Report Number
1056436-1996-00059
Event Type
Injury
Date Received
September 30, 1996
Date of Event
August 28, 1996
Report Date
September 27, 1996
Manufacturer
HORIZON MEDICAL PRODUCTS INC.
Product Code
LJT
Report Source
Manufacturer report
Reporter Location
VA, US
Reporter Occupation
PHYSICIAN

Narratives

Description of Event or Problem · 1

MD REMOVED DEVICE (SURGICALLY) BECAUSE IT WAS NOT WORKING. NO FURTHER INFO IS AVAILABLE.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1 TRIUMPH I PORT Implant VASCULAR ACCESS SYSTEM LJT HORIZON MEDICAL PRODUCTS INC. SSA-14-I NA

Patients

Seq Age Sex Outcome Treatment
1 57 YR Hospitalization| O