FDA Adverse Event Injury Summary report: N

ENDOWRIST

MDR report key: 20972823 · Received December 18, 2024

Report

Report Number
2955842-2024-23440
Event Type
Injury
Date Received
December 18, 2024
Date of Event
August 20, 2024
Report Date
November 19, 2024
Manufacturer
INTUITIVE SURGICAL, INC
Product Code
NAY
PMA / PMN Number
K214095
Removal / Correction Number
N/A
Adverse Event
Yes
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
VA, US
Reporter Occupation
003

Narratives

Additional Manufacturer Narrative · 0

INTUITIVE SURGICAL, INC. (ISI) RECEIVED THE FENESTRATED BIPOLAR FORCEPS INSTRUMENT TO PERFORM FAILURE ANALYSIS. THE INSTRUMENT WAS FOUND TO HAVE A BROKEN GRIP CABLE AT THE PROXIMAL CLEVIS HOLE. THE CABLE WAS FULLY BROKEN. THERE WAS NO DISCOLORATION, CORROSION, OR CONTAMINATION OF THE CABLE. FURTHER INSPECTION FOUND NO ABNORMALLY SHARP OR DAMAGED COMPONENTS.

Description of Event or Problem · 0

IT WAS REPORTED THAT DURING A DA VINCI-ASSISTED SURGICAL PROCEDURE, THE FENESTRATED BIPOLAR FORCEPS INSTRUMENT HAD A BROKEN WIRE. THE PROCEDURE WAS COMPLETED ROBOTICALLY. INTUITIVE SURGICAL, INC. (ISI) FOLLOWED UP WITH THE CUSTOMER AND OBTAINED THE FOLLOWING ADDITIONAL INFORMATION: A GENERAL REPORT WAS RECEIVED THAT DURING DA VINCI-ASSISTED SURGICAL PROCEDURES, THEY HAVE EXPERIENCED BROKEN FENESTRATED BIPOLAR FORCEPS INSTRUMENTS AT SEVERAL ASSOCIATED HOSPITALS. SPECIFIC EVENT AND DEVICE INFORMATION WAS NOT PROVIDED. IT WAS STATED THAT EACH PATIENT HAD INTRAOPERATIVE X-RAY IMAGING PERFORMED IN CASE A RETAINED PART OF THE WIRE DROPPED OFF IN THE PATIENT¿S CAVITY, WHICH THE CUSTOMER FELT WAS BECOMING A PATIENT SAFETY CONCERN.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
2283891 ENDOWRIST FENESTRATED BIPOLAR FORCEPS NAY INTUITIVE SURGICAL, INC 471205-17 K12240418 0263

Patients

Seq Age Sex Outcome Treatment
1 NA Unknown Required Intervention DA VINCI INSTRUMENTS AND ACCESSORIES.