FDA Adverse Event Malfunction Summary report: N

LIGASURE ADVANCE PISTOL GRIP

MDR report key: 2161765 · Received April 18, 2011

Report

Report Number
1717344-2011-00299
Event Type
Malfunction
Date Received
April 18, 2011
Date of Event
March 26, 2011
Report Date
March 26, 2011
Manufacturer
COVIDIEN LP (VALLEYLAB)
Product Code
GEI
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
OH, US
Reporter Occupation
OTHER

Narratives

Additional Manufacturer Narrative · 1

(B)(4). THE INCIDENT DEVICE HAS BEEN RECEIVED AND IS UNDER EVAL. WHEN THE DEVICE EVAL IS COMPLETE, A F/U REPORT WILL BE SUBMITTED.

Description of Event or Problem · 1

THE CUSTOMER REPORTED THAT THE INSULATION SLEEVE CAME OFF OF THE DEVICE AND INTO THE PT CAVITY. THE SLEEVE WAS RECOVERED AND THERE WAS NO PT INJURY.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1 LIGASURE ADVANCE PISTOL GRIP LIGASURE VESSEL SEALING SYSTEM GEI COVIDIEN LP (VALLEYLAB) 202997

Patients

Seq Age Sex Outcome Treatment
1 UNK