FDA Adverse Event Malfunction Summary report: N

SENHANCE

MDR report key: 21987574 · Received May 8, 2025

Report

Report Number
3007593944-2025-00001
Event Type
Malfunction
Date Received
May 8, 2025
Date of Event
April 16, 2025
Report Date
May 8, 2025
Manufacturer
ASENSUS SURGICAL, INC.
Product Code
NAY
UDI-DI
00815440021894
PMA / PMN Number
K171120
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
IL, US
Reporter Occupation
003

Narratives

Description of Event or Problem · 0

DATE OF INCIDENT: (B)(6) 2025. LOCATION: (B)(6). DEVICE: MONOPOLAR L-HOOK INSTRUMENT (X0007177). NO INJURY OCCURRED TO A PATIENT OR USER. IT WAS REPORTED THAT DURING A ROBOTICALLY-ASSISTED LAPAROSCOPIC CHOLECYSTECTOMY PROCEDURE, A MATERIAL SEPARATION OCCURRED INVOLVING A MONOPOLAR L-HOOK INSTRUMENT. WHILE THE ROBOTIC SURGICAL SYSTEM WAS MANEUVERING THE INSTRUMENT TO FACILITATE CONTINUED DISSECTION OF THE GALLBLADDER FROM THE LIVER BED, THE L-HOOK DETACHED FROM THE ADAPTER AND DESCENDED INTO THE PATIENT'S ABDOMEN WITHOUT DIRECT SURGEON COMMAND. SUBSEQUENT BEDSIDE EXAMINATION REVEALED THAT THE L-HOOK HAD SEPARATED FROM THE ADAPTER WHILE THE ADAPTER REMAINED AFFIXED TO THE MANIPULATOR ARM. THE DETACHED L-HOOK WAS OBSERVED SUSPENDED WITHIN THE TROCAR UNTIL MANUALLY AND FULLY RETRIEVED BY THE BEDSIDE ASSISTANT. EXAMINATION OF THE ABDOMINAL CAVITY INDICATED NO APPARENT CONTACT BETWEEN THE DETACHED L-HOOK AND ANY ANATOMICAL STRUCTURES. THE SURGICAL PROCEDURE EXPERIENCED A DELAY OF LESS THAN 15 MINUTES AS A RESULT OF THIS EVENT. THE ATTENDING SURGEON REPORTED NO CONCERNS REGARDING POTENTIAL TISSUE INJURY RELATED TO THE DEVICE MALFUNCTION. AN INVESTIGATION INTO THE CAUSE OF THE MATERIAL SEPARATION WAS COMPLETED. IMMEDIATE DISPOSAL PREVENTED EXTENSIVE DEVICE INVESTIGATION AND LOT NUMBER CONFIRMATION. HOWEVER, THE INVESTIGATION THAT WAS COMPLETED REVEALED THAT THE SALES SUPPORT REPRESENTATIVE CONFIRMED PROPER L-HOOK ASSEMBLY UNDER ASENSUS EMPLOYEE SUPERVISION, FUNCTIONING FOR 20 MINUTES BEFORE SPONTANEOUS DISASSEMBLY. THE REPRESENTATIVE NOTED THE INSTRUMENT'S AGE AND HEAVY USE, SUSPECTING A BROKEN PLASTIC SHEATH SECURING THE FASTENING CAP LED TO SHAFT BREAKAGE, INSTABILITY, INCREASED FORCE ON THE METAL CYLINDER INTERFACE, AND SUBSEQUENT INSTRUMENT SLIPPAGE ONCE THE CYLINDER DETACHED. THE PRODUCT IFU INDICATES THAT SENHANCE PASSIVE/MONOPOLAR INSTRUMENT LIFESPAN DEPENDS ON WEAR/DAMAGE FROM USE/HANDLING AND SHOULD BE INSPECTED PRIOR TO USE. THIS INSPECTION REQUIREMENT MUST VERIFY PROPER FUNCTION, STRAIGHTNESS, JAW ALIGNMENT, INSULATION INTEGRITY, AND ABSENCE OF DAMAGE. GIVEN THIS INFORMATION, THE ROOT CAUSE IS UNCONFIRMED. POTENTIAL CONTRIBUTING FACTORS INCLUDE DEVICE WEAR AND TEAR, OVERUSE, AND WELD FAILURE AT THE METAL CYLINDER-SHAFT CONNECTION (DUE TO WEAR), LEADING TO SHAFT BREAKAGE AND DISASSEMBLY. THIS EVENT, BEING THE FIRST RECORDED INSTANCE AT THE SITE OF AN INSTRUMENT SHAFT DETACHMENT FROM AN ADAPTER DURING A SURGICAL CASE, WILL BE TRACKED AND TRENDED FOR ANALYSIS.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
761086 SENHANCE X0007177, MONOPOLAR L-HOOK ELECTRODE, 5 MM X 310 MM NAY ASENSUS SURGICAL, INC. X0007177 139730 00815440021894

Patients

Seq Age Sex Outcome Treatment
1 NA Unknown