FDA Adverse Event Other Summary report: N

CONMED

MDR report key: 530897 · Received March 2, 2004

Report

Report Number
1720159-2004-00003
Event Type
Other
Date Received
March 2, 2004
Manufacturer
CONMED ELECTROSURGERY
Product Code
GEI
Removal / Correction Number
NA
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
AR, US
Reporter Occupation
OTHER

Narratives

Description of Event or Problem · 1

PENCIL CAUSED A BURN WHERE IT WAS LAYING AGAINST THE LIP.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1 CONMED ELECTROSURGICAL PENCIL GEI CONMED ELECTROSURGERY NA 030819-1

Patients

Seq Age Sex Outcome Treatment
1 NA