FDA Adverse Event Other Summary report: N

ELMED

MDR report key: 174285 · Received June 25, 1998

Report

Report Number
174285
Event Type
Other
Date Received
June 25, 1998
Date of Event
November 21, 1997
Report Date
June 23, 1998
Manufacturer
*
Product Code
KNS
Adverse Event
Yes
Report Source
User Facility report
Reporter Location
CT, US
Reporter Occupation
RISK MANAGER

Narratives

Description of Event or Problem · 1

WHILE CAUTERIZING GALL BLADDER, SPARKS FROM INSULATED PORTION OF "L" HOOK BURNED LIVER.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1 ELMED "L" HOOK CAUTERY KNS * * *

Patients

Seq Age Sex Outcome Treatment
1 40 YR Other