FDA Adverse Event Malfunction Summary report: N

DRIVER SHAFT, T6, SELF RETAINING, AO

MDR report key: 20470773 · Received October 17, 2024

Report

Report Number
1220246-2024-08181
Event Type
Malfunction
Date Received
October 17, 2024
Date of Event
September 19, 2024
Report Date
January 24, 2025
Manufacturer
ARTHREX, INC.
Product Code
LXH
UDI-DI
00888867385566
PMA / PMN Number
EXEMPT
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
FL, US
Reporter Occupation
501

Narratives

Additional Manufacturer Narrative · 0

ADDITIONAL INFORMATION: D9, G3, H3, H6. COMPLAINT ALLEGATION IS CONFIRMED. UPON VISUAL INSPECTION, IT WAS NOTED THAT THE DRIVE GEOMETRY AT THE DISTAL TIP OF THE DRIVER SHAFT, T6, AO HAD BROKEN OFF AND TWISTED. NO BROKEN PIECES WERE RETURNED FOR INVESTIGATION. FUNCTIONAL TESTING WAS NOT PERFORMED DUE TO THE DAMAGE TO THE DEVICE. THE MOST LIKELY CAUSE IS ATTRIBUTED TO USER ERROR DUE TO OVER-TORQUING/OVER-ENGAGING THE DRIVER WITHIN THE SCREW HEAD. PER DFU-0023-12 REV 0 CAUTIONS- TO AVOID DAMAGING THE INSTRUMENTS, DO NOT IMPACT OR SUBJECT TO BLUNT FORCE ANY INSTRUMENTS THAT ARE DESIGNED TO BE TURNED OR SCREWED IN. WHEN TWO DEVICES ARE INTENDED TO BE THREADED TOGETHER, ENSURE THAT THEY ARE FULLY ENGAGED PRIOR TO USE.

Additional Manufacturer Narrative · 0

INVESTIGATION IS IN PROCESS. A FOLLOW-UP REPORT WILL BE PROVIDED UPON AVAILABILITY OF ADDITIONAL INFORMATION.

Description of Event or Problem · 0

ON (B)(6) 2024 , IT WAS REPORTED BY A SALES REPRESENTATIVE VIA SEMS-06672663 THAT AN AR-18800-03 DRIVER SHAFT TIP BROKE OFF INSIDE THE PATIENT WHILE INSERTING THE SCREW, AND AN AR-18800-03 DRIVER SHAFT WAS WARPED. THE CASE WAS NOT AFFECTED. THIS WAS DISCOVERED DURING A PROCEDURE ON (B)(6) 2024 , WITH NO REPORTED PATIENT HARM. ADDITIONAL INFORMATION HAS BEEN REQUESTED.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1203415 DRIVER SHAFT, T6, SELF RETAINING, AO ORTHOPEDIC MANUAL SURG INSTR LXH ARTHREX, INC. DRIVER SHAFT, T6, SELF RETAINING, AO 1392347 00888867385566

Patients

Seq Age Sex Outcome Treatment
1 NA Unknown