FDA Adverse Event Malfunction Summary report: N

ULTRACISION HARMONIC ACE

MDR report key: 2002735 · Received February 28, 2011

Report

Report Number
3005075853-2011-00768
Event Type
Malfunction
Date Received
February 28, 2011
Date of Event
February 14, 2011
Report Date
February 15, 2011
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
JA
Reporter Occupation
OTHER

Narratives

Additional Manufacturer Narrative · 1

(B)(4). THE DEVICE WAS RETURNED WITH THE DISTAL TIP OF THE BLADE BROKEN OFF AND RETURNED WITH THE DEVICE. THE REMAINING BLADE PORTION WAS SCRATCHED. THE DEVICE WAS ACTIVATED WITH THE GENERATOR AND AN ERROR CODE 5 WAS DISPLAYED. PROBABLE CAUSES OF BLADE DAMAGE, INCLUDING BREAKAGE, ARE EXTERNAL CONTACT DURING PRE-OP OR GENERAL USE, BLADE CONTACT WITH OTHER DEVICES, STAPLES OR CLIPS DURING THE PROCEDURE OR USING ANY MEANS OTHER THAN THE BLADE WRENCH TO ATTACH OR DETACH THE BLADE. ONCE MINOR BLADE DAMAGE HAS OCCURRED, SUBSEQUENT ACTIVATIONS MAY INCREASE DAMAGE SEVERITY AND RESULT IN AN ERROR CODE 5 OR BLADE "LOCKOUT" LATER IN THE PROCEDURE, AND CONTINUED USAGE CAN RESULT IN A BROKEN BLADE.

Additional Manufacturer Narrative · 1

(B)(4). INFORMATION ANTICIPATED, BUT UNAVAILABLE AT THIS TIME

Description of Event or Problem · 1

IT WAS REPORTED THAT DURING A LAPAROSCOPIC APPENDECTOMY PROCEDURE, AN ERROR SOUND WAS HEARD DURING USE AND THE DEVICE BECAME NOT TO BE ACTIVATED. WHEN THE BLADE WAS WIPED WITH THE GAUZE, THE TIP OF THE BLADE WAS BROKEN OFF. THE BROKEN PIECES WERE RETRIEVED. AS THE BLADE WAS BROKEN OFF OUTSIDE THE PATIENT, NO PIECES WERE LEFT INSIDE THE PATIENT'S BODY.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1 ULTRACISION HARMONIC ACE INSTRUMENT, ULTRASONIC SURGICAL LFL ETHICON ENDO-SURGERY, LLC. UNK G9LC4E

Patients

Seq Age Sex Outcome Treatment
1 GENERATOR AND HANDPIECE