FDA Adverse Event Malfunction Summary report: N

CARDINAL MEDICAL

MDR report key: 1951043 · Received December 22, 2010

Report

Report Number
MW5018842
Event Type
Malfunction
Date Received
December 22, 2010
Manufacturer
CARDINAL HEALTH
Product Code
GEI
Product Problem
Yes
Report Source
Voluntary report
Reporter Location
KY, US
Reporter Occupation
RISK MANAGER

Narratives

Description of Event or Problem · 1

BURNING PHYSICIAN'S HAND WHILE IN USE.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1 CARDINAL MEDICAL BOVIE PEN GEI CARDINAL HEALTH

Patients

Seq Age Sex Outcome Treatment
1 36 YR Other