FDA Adverse Event Summary report: N

LIGASURE IMPACT

MDR report key: 1883515 · Received October 18, 2010

Report

Report Number
1883515
Date Received
October 18, 2010
Date of Event
October 15, 2010
Report Date
October 18, 2010
Manufacturer
COVIDIEN VALLEYLAB
Product Code
GEI
Report Source
User Facility report
Reporter Location
MO, US

Narratives

Description of Event or Problem · 1

JAWS WOULD NOT OPEN. THEY WERE STUCK TOGETHER AFTER TWO HOURS OF USE. DEVICE TAKEN OFF THE FIELD AND CLEANED TO BE SENT FOR EVALUATION.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1 LIGASURE IMPACT TISSUE FUSION SYSTEM GEI COVIDIEN VALLEYLAB * *

Patients

Seq Age Sex Outcome Treatment
1 73 YR