FDA Adverse Event Malfunction Summary report: N

CONMED CORPORATION

MDR report key: 451240 · Received March 21, 2003

Report

Report Number
1720159-2003-00017
Event Type
Malfunction
Date Received
March 21, 2003
Date of Event
February 1, 2003
Report Date
February 25, 2003
Manufacturer
CONMED ELECTROSURGERY
Product Code
GEI
Removal / Correction Number
NA
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
TX, US
Reporter Occupation
OTHER

Narratives

Description of Event or Problem · 1

A DOCTOR HAS BEEN BURNED ON THE HIP SERVERAL TIMES USING DIFFERENT MACHINES. THIS TIME IT WAS THE EXCALIBUR PLUS PC.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1 CONMED CORPORATION ELECTROSURGICAL UNIT GEI CONMED ELECTROSURGERY EXCALIBUR PLUS PC NA

Patients

Seq Age Sex Outcome Treatment
1 NA Other