FDA Adverse Event Malfunction Summary report: N

MONOPOLAR CURVED SCISSORS INSTRUMENT

MDR report key: 3382471 · Received October 2, 2013

Report

Report Number
2955842-2013-03938
Event Type
Malfunction
Date Received
October 2, 2013
Date of Event
August 16, 2013
Report Date
September 4, 2013
Manufacturer
INTUITIVE SURGICAL,INC.
Product Code
NAY
PMA / PMN Number
K050005
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
FL
Reporter Occupation
OTHER

Narratives

Additional Manufacturer Narrative · 1

THE INSTRUMENT WAS RETURNED AND EVALUATED. FAILURE ANALYSIS WAS UNABLE TO CONFIRM THE REPORTED COMPLAINT. ALTHOUGH THE GRIP WERE ABLE TO SEPARATE, THERE WAS SOME UNUSUAL, WHITE COLORED RESIDUE AT THE END OF THE BLADES. FAILURE ANALYSIS CONCLUDED THE DAMAGE WAS LIKELY DUE TO IMPROPER CLEANING. AN ADDITIONAL FINDING WAS VARIOUS SCRATCHES ON THE DISTAL END OF THE MAIN TUBE SHOWING LIGHT MATERIAL REMOVAL AND A ROUGH SURFACE FINISH. THE SCRATCHES WERE .060 - .170 IN LENGTH AND NOT AXIALLY ALIGNED WITH THE TUBE. FAILURE ANALYSIS CONCLUDED THE DAMAGE MAY BE DUE TO MISHANDLING / MISUSE. NO OTHER DAMAGE WAS FOUND. THE INSTRUMENTS AND ACCESSORIES USER MANUAL SPECIFICALLY STATES: WARNING: READ ALL INSTRUCTIONS CAREFULLY. FAILURE TO PROPERLY FOLLOW INSTRUCTIONS MAY CAUSE IMPROPER FUNCTIONING OF THE DEVICE. THE CUSTOMER REPORTED COMPLAINT DOES NOT ITSELF CONSTITUTE A MDR REPORTABLE EVENT; HOWEVER; TUBE ABRASIONS WITH MATERIAL REMOVED, FOUND DURING FAILURE ANALYSIS EVALUATION COULD LIKELY CAUSE OR CONTRIBUTE TO AN ADVERSE EVENT IF THE FAILURE MODE WERE TO RECUR.

Description of Event or Problem · 1

IT WAS REPORTED THAT DURING REPROCESSING, THE JAWS OF A MONOPOLAR CURVED SCISSORS INSTRUMENT WOULD NOT OPEN WHEN THEY TRIED TO CLEAN THEM. THERE WERE NO MISSING PIECES OR FALLEN PIECES REPORTED. NO PATIENT HARM, ADVERSE OUTCOME, OR INJURY WAS REPORTED.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
498657 MONOPOLAR CURVED SCISSORS INSTRUMENT ENDOSCOPIC ELECTROSURGICAL INSTRUMENT NAY INTUITIVE SURGICAL,INC. 420179-12 M12130626 198

Patients

Seq Age Sex Outcome Treatment
1 DA VINCI SI SYSTEM INSTRUMENTS & ACCESSORIES, ESU