FDA Adverse Event Malfunction Summary report: N

HARMONIC ACE 36CM W ERG HANDLE

MDR report key: 1112786 · Received August 12, 2008

Report

Report Number
3005075853-2008-01136
Event Type
Malfunction
Date Received
August 12, 2008
Date of Event
July 29, 2008
Report Date
July 29, 2008
Manufacturer
ETHICON ENDO-SURGERY, LLC
Product Code
LFL
PMA / PMN Number
K042777
Removal / Correction Number
NA
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
VA, US
Reporter Occupation
OTHER

Narratives

Additional Manufacturer Narrative · 1

D4, H4, 6: INFO IS ANTICIPATED, BUT UNAVAILABLE AT THIS TIME.

Description of Event or Problem · 1

IT WAS REPORTED THAT DURING A LAP OOPHORECTOMY PROCEDURE, THE ACTIVE BLADE BROKE OFF OUTSIDE OF THE PT. THE PROCEDURE WAS NEAR COMPLETION, NO NEED TO OPEN A NEW DEVICE. THERE WAS NO PT CONSEQUENCE. THE PT IS CURRENTLY STABLE.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1 HARMONIC ACE 36CM W ERG HANDLE LFL ETHICON ENDO-SURGERY, LLC NA E4L54V

Patients

Seq Age Sex Outcome Treatment
1 HANDPIECE| GENERATOR