FDA Adverse Event Malfunction Summary report: N

HARMONIC FOCUS* CURVED SHEARS, TORQUE WRENCH AND GRIP ASSIST

MDR report key: 3133853 · Received May 29, 2013

Report

Report Number
3005075853-2013-02624
Event Type
Malfunction
Date Received
May 29, 2013
Date of Event
May 9, 2013
Report Date
May 13, 2013
Manufacturer
ETHICON ENDO-SURGERY, LLC.
Product Code
LFL
PMA / PMN Number
K063192
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 RECEIVED WITH THE HANDLE BROKEN. IN ADDITION THE BLADE WAS FOUND BROKEN AND NOT RETURNED. FUNCTIONAL TESTING COULD NOT BE PERFORMED DUE TO THE RETURNED CONDITION OF THE DEVICE. NO CONCLUSION COULD BE REACHED HOW THE HANDLE WAS BROKEN. PLEASE NOTE THAT THIS CONDITION IS UNRELATED WITH THE EVENT REPORTED. IT SHOULD BE NOTED THAT AS PART OF OUR QUALITY PROCESS, EACH DEVICE IS VISUALLY INSPECTED AND FUNCTIONALLY TESTED DURING MANUFACTURING TO ENSURE THE DEVICE MEETS THE REQUIRED SPECIFICATIONS PRIOR TO SHIPMENT.

Additional Manufacturer Narrative · 1

(B)(4). WHEN ADDITIONAL INFORMATION IS RECEIVED AND/OR THE DEVICE ANALYSIS HAS BEEN COMPLETED, A SUPPLEMENTAL MEDWATCH WILL BE SENT.

Description of Event or Problem · 1

IT WAS REPORTED THAT DURING AN UNKNOWN PROCEDURE, AN ERROR OCCURRED. THE ERROR CODE WAS UNKNOWN. THE BLADE WAS BROKEN OFF OUTSIDE OF THE PATIENT AFTER THE ERRORS. NO PIECES FELL INTO THE PATIENT. ANOTHER DEVICE WAS USED TO COMPLETE THE CASE. THERE WERE NO ADVERSE CONSEQUENCES TO THE PATIENT. ONE DEVICE WILL BE RETURNING.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
236664 HARMONIC FOCUS* CURVED SHEARS, TORQUE WRENCH AND GRIP ASSIST INSTRUMENT, ULTRASONIC SURGICAL LFL ETHICON ENDO-SURGERY, LLC. UNK UNK

Patients

Seq Age Sex Outcome Treatment
1 GENERATOR AND HANDPIECE