FDA Adverse Event Death Summary report: N

HEM-O-LOK L LIGATION CLIPS

MDR report key: 640738 · Received October 14, 2005

Report

Report Number
1044475-2005-00015
Event Type
Death
Date Received
October 14, 2005
Date of Event
September 1, 2005
Report Date
October 14, 2005
Manufacturer
WECK, TELEFLEX MEDICAL
Product Code
FZP
Removal / Correction Number
NA
Adverse Event
Yes
Report Source
Manufacturer report
Reporter Location
FR
Reporter Occupation
RISK MANAGER

Narratives

Description of Event or Problem · 1

PROCEDURE: LAPAROSCOPIC NEPHRECTOMY. WECK, TELEFLEX MEDICAL RECEIVED NOTICE THAT A PT WHO UNDERWENT A LAPAROSCOPIC NEPHRECTOMY DIED A FEW HOURS PAST OPERATION. NO ADDITIONAL INFORMATION REGARDING SITE OF LIGATION OR CAUSE OF DEATH HAS BEEN RECEIVED.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1 HEM-O-LOK L LIGATION CLIPS LARGE POLYMER LIGATION CLIPS FZP WECK, TELEFLEX MEDICAL NA 1997116

Patients

Seq Age Sex Outcome Treatment
1 UNKNOWN Death