FDA Adverse Event Malfunction Summary report: N

ENDOWRIST;DAVINCI SI

MDR report key: 14247569 · Received April 29, 2022

Report

Report Number
2955842-2022-11311
Event Type
Malfunction
Date Received
April 29, 2022
Date of Event
August 14, 2019
Report Date
March 29, 2022
Manufacturer
INTUITIVE SURGICAL, INC
Product Code
NAY
UDI-DI
00886874111505
PMA / PMN Number
K180033
Removal / Correction Number
N/A
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
JA
Reporter Occupation
003

Narratives

Additional Manufacturer Narrative · 0

INTUITIVE SURGICAL, INC. (ISI) RECEIVED THE MONOPOLAR CURVED SCISSORS ASSOCIATED WITH THE COMPLAINT AND COMPLETED THE INVESTIGATION. FAILURE ANALYSIS INVESTIGATIONS REPLICATED AND CONFIRMED THE CUSTOMER REPORTED COMPLAINT OF DAMAGED CABLE AT TIP. FAILURE ANALYSIS FOUND THE PRIMARY FAILURE OF BROKEN GRIP CABLE. THE INSTRUMENT WAS FOUND TO HAVE A BROKEN GRIP CABLE AT THE DISTAL IDLER PULLEY. THE DISTAL IDLER PULLEY SPUN FREELY AND DID NOT EXHIBIT ANY DAMAGE. ROOT CAUSE OF BROKEN GRIP CABLE IS ATTRIBUTED TO A COMPONENT FAILURE. ADDITIONAL OBSERVATION NOT REPORTED BY SITE: THE INSTRUMENT WAS FOUND TO HAVE THERMAL DAMAGE ON THE ORANGE TUBE EXTENSION AT THE DISTAL END. ROOT CAUSE IS ATTRIBUTED TO MISHANDLING/MISUSE. A REVIEW OF THE SITE'S COMPLAINT HISTORY DOES NOT SHOW ANY ADDITIONAL COMPLAINTS RELATED TO THIS PRODUCT AND/OR THIS EVENT. A REVIEW OF THE INSTRUMENT LOG FOR PART# 420179-22/LOT# N11181017 0768 ASSOCIATED WITH THIS EVENT HAS BEEN PERFORMED. PER LOGS, THE MONOPOLAR CURVED SCISSORS WAS LAST USED ON (B)(6) 2019 ON SYSTEM (B)(4) WITH 3 LIVES REMAINING. THE REVIEW OF THE PROVIDED IMAGE CONFIRMED THE DAMAGED CABLE. BASED ON THE ADDITIONAL INFORMATION OBTAINED FROM FAILURE ANALYSIS INVESTIGATION, THIS COMPLAINT IS BEING REPORTED DUE TO THE FOLLOWING CONCLUSION: IT WAS ALLEGED THAT THE INSTRUMENT EXHIBITED SIGNS INDICATIVE OF THERMAL DAMAGE. AT THIS TIME, IT IS UNKNOWN WHAT CAUSED THE THERMAL DAMAGE TO OCCUR. WHILE THERE WAS NO HARM OR INJURY TO THE PATIENT, THE REPORTED FAILURE MODE COULD LIKELY CAUSE OR CONTRIBUTE TO AN ADVERSE EVENT IF IT WERE TO RECUR.

Description of Event or Problem · 0

IT WAS REPORTED THAT DURING DA VINCI-ASSISTED SURGICAL PROCEDURE, THE MONOPOLAR CURVED SCISSORS WAS FOUND TO HAVE A DAMAGED CABLE AT THE TIP. A BACKUP INSTRUMENT OF THE SAME KIND WAS USED TO CONTINUE. THE PROCEDURE WAS COMPLETED WITH NO REPORTED INJURY. INTUITIVE SURGICAL, INC. (ISI) FOLLOWED UP WITH THE INITIAL REPORTER TO OBTAIN THE INFORMATION REGARDING PATIENT DEMOGRAPHICS, RELEVANT TESTING, AND MEDICAL HISTORY; HOWEVER, THE REPORTER WAS NOT ABLE TO PROVIDE THAT INFORMATION. PER CUSTOMER, THE MONOPOLAR CURVED SCISSORS WAS INSPECTED PRIOR TO USE AND NO ANOMALY WAS NOTED. THERE WAS NO REPORT OF ANY COLLISION OR ARCING.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
204030 ENDOWRIST;DAVINCI SI MONOPOLAR CURVED SCISSORS NAY INTUITIVE SURGICAL, INC 420179-22 N11181017 0768 00886874111505

Patients

Seq Age Sex Outcome Treatment
1 Unknown DA VINCI INSTRUMENTS AND ACCESSORIES