FDA Adverse Event Malfunction Summary report: N

LIGASURE ADVANCE PISTOL GRIP

MDR report key: 3192566 · Received June 19, 2013

Report

Report Number
1717344-2013-00434
Event Type
Malfunction
Date Received
June 19, 2013
Date of Event
May 20, 2013
Report Date
May 24, 2013
Manufacturer
COVIDIEN LP
Product Code
GEI
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
CA, US
Reporter Occupation
OTHER

Narratives

Additional Manufacturer Narrative · 1

(B)(4). THE KNIFE DID NOT ADVANCE WHEN THE TRIGGER WAS ACTIVATED AND IT WAS FOUND THAT THE KNIFE WAS HITTING THE BACK OF THE BLUE JAW SEAL PLATE. THE KNIFE EDGE WAS DAMAGED WHEN IT CONTACTED THE SEAL PLATE. THE KNIFE WAS STILL WITHIN THE JAWS, BUT THE WEBBING WAS PROTRUDING FROM BOTH SIDES OF THE HINGE AREA AND WAS NOT SHARP. THE KNIFE HITTING THE SEAL PLATE CAUSED THE WEBBING TO PROTRUDE. A PRODUCTION SCREENING FIXTURE AND A DEEPER KNIFE SLOT IN THE JAW WERE PUT IN PLACE TO HELP MITIGATE THE OCCURRENCE OF THE KNIFE HITTING THE BACK OF THE SEAL PLATE.

Description of Event or Problem · 1

THE CUSTOMER REPORTED THAT THE KNIFE BLADE JAMMED AFTER MANY USES. THERE WAS NO INJURY TO THE PT. THE DEVICE WAS RETURNED FOR INVESTIGATION AND VISUAL INSPECTION NOTED THAT THE WEBBING WAS PROTRUDING FROM THE HINGE.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
279026 LIGASURE ADVANCE PISTOL GRIP LIGASURE VESSEL SEALING SYSTEM GEI COVIDIEN LP 249952X

Patients

Seq Age Sex Outcome Treatment
1