FDA Adverse Event Injury Summary report: N

PERFECTEMP BATTERY OPERATED CAUTERY

MDR report key: 282992 · Received June 23, 2000

Report

Report Number
1030322-2000-00002
Event Type
Injury
Date Received
June 23, 2000
Date of Event
April 19, 2000
Report Date
June 2, 2000
Manufacturer
AARON MEDICAL INDUSTRIES
Product Code
GEI
Report Source
Manufacturer report
Reporter Location
MO, US
Reporter Occupation
NURSE

Narratives

Description of Event or Problem · 1

INTRAOPERATIVE FLASH FIRE DURING ECTROPIAN REPAIR OF EYELID RESULTING IN 2ND DEGREE FACIAL BURN. PT EXPIRED ON 5/4/00.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1 PERFECTEMP BATTERY OPERATED CAUTERY BATTERY OPERATED CAUTERY GEI AARON MEDICAL INDUSTRIES * 1299C

Patients

Seq Age Sex Outcome Treatment
1 84 YR Required Intervention MASK AND STERILE DRAPE.| OXYGEN, STERILE GOWN AND DRAPE (PAPER) BREATHING