FDA Adverse Event Summary report: N

FORCE TRIVERSE

MDR report key: 1840269 · Received September 13, 2010

Report

Report Number
1840269
Date Received
September 13, 2010
Date of Event
September 2, 2010
Report Date
September 13, 2010
Manufacturer
COVIDIEN
Product Code
GEI
Report Source
User Facility report
Reporter Location
MO, US
Reporter Occupation
RISK MANAGER

Narratives

Description of Event or Problem · 1

THE CIRCULATING RN WENT TO PLUG IN THE FORCE TRIVERSE HANDPIECE INTO THE TRIAD MACHINE AND THE CONNECTION SNAPPED.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1 FORCE TRIVERSE ELECTROSURGICAL HANDPIECE GEI COVIDIEN UNK UNK

Patients

Seq Age Sex Outcome Treatment
1 66 YR