FDA Adverse Event Malfunction Summary report: N

MONOPOLAR CURVED SCISSORS INSTRUMENT

MDR report key: 3163538 · Received June 11, 2013

Report

Report Number
2955842-2013-02106
Event Type
Malfunction
Date Received
June 11, 2013
Date of Event
May 16, 2013
Report Date
June 14, 2013
Manufacturer
INTUITIVE SURGICAL,INC.
Product Code
NAY
PMA / PMN Number
K050005
Removal / Correction Number
2955842-051613-005
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
DC
Reporter Occupation
OTHER

Narratives

Additional Manufacturer Narrative · 1

THE INSTRUMENT AND/OR ACCESSORY HAVE NOT BEEN RETURNED FOR EVALUATION; THEREFORE, THE ROOT CAUSE OF THE CUSTOMER REPORTED FAILURE MODE CANNOT BE DETERMINED. A FOLLOW-UP MDR WILL BE SUBMITTED IF THE INSTRUMENT IS RETURNED (POST ENGINEERING EVALUATION), OR IF ADDITIONAL INFORMATION IS RECEIVED. THE CUSTOMER REPORTED COMPLAINT DOES NOT ITSELF CONSTITUTE A MDR REPORTABLE EVENT; HOWEVER, THE REPORTED MALFUNCTION IF TO RECUR COULD CAUSE OR CONTRIBUTE TO AN ADVERSE EVENT.

Additional Manufacturer Narrative · 1

(B)(4). NO OTHER DAMAGE FOUND. RECURRENCE OF THE ALLEGED FAILURE MODE IS NOT EXPECTED TO CAUSE OR CONTRIBUTE TO A DEATH, SERIOUS INJURY OR SERIOUS DETERIORATION IN THE STATE OF HEALTH OF A PATIENT. BASED ON THIS ADDITIONAL FAILURE ANALYSIS INVESTIGATION INFORMATION, THIS MDR REPORT IS BEING RETRACTED.

Description of Event or Problem · 1

IT WAS REPORTED THAT PRIOR TO STARTING A DA VINCI S SURGICAL PROCEDURE THE MONOPOLAR CURVED SCISSORS INSTRUMENT (MCS) ORANGE SLEEVE ON THE DISTAL END OF THE INSTRUMENT WAS NOTED TO BE CRACKED. NO PATIENT HARM, ADVERSE OUTCOME OR INJURY WAS REPORTED.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
264474 MONOPOLAR CURVED SCISSORS INSTRUMENT ENDOSCOPIC ELECTROSURGICAL INSTRUMENT NAY INTUITIVE SURGICAL,INC. 420179-10 M13130111 456

Patients

Seq Age Sex Outcome Treatment
1 DAVINCI S SYSTEM, ESU, INSTRUMENTS & ACCESSORIES