FDA Adverse Event Malfunction Summary report: N

HARMONIC ACE ATT

MDR report key: 4182436 · Received October 17, 2014

Report

Report Number
3005075853-2014-07209
Event Type
Malfunction
Date Received
October 17, 2014
Date of Event
April 24, 2014
Report Date
April 24, 2014
Manufacturer
ETHICON ENDO-SURGERY, LLC.
Product Code
LFL
PMA / PMN Number
K120729
Removal / Correction Number
NA
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
FR
Reporter Occupation
OTHER

Narratives

Additional Manufacturer Narrative · 1

(B)(4). SHOULD THE INFORMATION BE PROVIDED LATER, A SUPPLEMENTAL MEDWATCH WILL BE SENT. THE DEVICE WAS RECEIVED WITH THE HAND ACTIVATIONS CONTACTS BENT. THE DEVICE WAS CONNECTED TO A TEST HANDPIECE WITH DIFFICULTY. DURING MECHANICAL TESTING, THE ROTATION KNOB DID NOT ROTATE FREELY. THE DEVICE WAS THEN FUNCTIONALLY TESTED ON THE GEN11 GENERATOR. DURING FUNCTIONAL TESTING, NO ALERT SCREENS WERE DISPLAYED. THE DAMAGED HAND ACTIVATION CONTACTS COULD CAUSE ROTATIONAL ISSUES WITH THE DEVICE. IN ADDITION, IT CAN CAUSE IMPROPER TORQUING OF THE BLADE, WHICH COULD CAUSE THE GENERATOR TO DISPLAY COMMUNICATION OR ACTIVATION ISSUES AND ALERT SCREENS. TO AVOID DAMAGING THE CONTACTS, IT IS RECOMMENDED TO ASSEMBLE THE DEVICE VERTICALLY. HAND SWITCH CONTACTS DAMAGED DUE TO TILTED HANDPIECE HITTING CONTACT TOP SURFACE DURING ASSEMBLY.

Description of Event or Problem · 1

IT WAS REPORTED THAT DURING AN UNKNOWN PROCEDURE, THE INSTRUMENT HAD PROBLEM ON ROTATION KNOB. CUSTOMER CANNOT PROVIDE ANY MORE DETAILS ABOUT THE CIRCUMSTANCES IN WHICH THE ISSUE OCCURRED. NO PATIENT CONSEQUENCE WAS REPORTED. ONE DEVICE IS BEING RETURNED.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
662195 HARMONIC ACE ATT INSTRUMENT, ULTRASONIC SURGICAL LFL ETHICON ENDO-SURGERY, LLC. NA UNK

Patients

Seq Age Sex Outcome Treatment
1 GENERATOR AND HANDPIECE