FDA Adverse Event Malfunction Summary report: N

T20 HEXALOBE DRIVER

MDR report key: 24251575 · Received February 3, 2026

Report

Report Number
1220246-2026-00387
Event Type
Malfunction
Date Received
February 3, 2026
Date of Event
November 20, 2025
Report Date
February 3, 2026
Manufacturer
ARTHREX, INC.
Product Code
MDM
UDI-DI
00888867133747
PMA / PMN Number
EXEMPT
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
SW
Reporter Occupation
501

Narratives

Additional Manufacturer Narrative · 0

THE REPORTED EVENT WAS CONFIRMED AS ONE UNPACKAGED AR-8970-03, T20 HEXALOBE DRIVER, BATCH NUMBER 1392436, WAS RECEIVED FOR INVESTIGATION AND THE EVALUATION REVEALED THAT A PART OF THE HEXALOBE TIP IS BROKEN OFF (SEE EVALUATION PICTURES 3 + 4). FUNCTIONAL TESTING WAS NOT PERFORMED DUE TO THE DAMAGE OF THE DEVICE. NO FRAGMENTS WERE RETURNED FOR EVALUATION. THE MOST LIKELY CAUSE FOR THE REPORTED FAILURE CAN BE ATTRIBUTED TO USER ERROR OF THE DEVICE DUE TO PRYING/LEVERAGING THE DRIVER WHILE ENGAGED WITH THE SCREW AND/OR OVER-TORQUING/OVER-ENGAGING THE DRIVER WITH THE SCREW HEAD.

Description of Event or Problem · 0

IT WAS REPORTED THAT DURING A SURGERY THE SCREWDRIVERS WERE HEAVILY WORN. PER COMPLAINT REPORTER THERE WAS NO HARM FOR PATIENT, OPERATOR OR THIRD PARTY. NO FURTHER INFORMATION RECEIVED. UPDATE 14-JAN-2026: THE REPORTED DEVICES ARRIVED AT ARTHREX GMBH AND DURING AN INITIAL INSPECTION OF THE DEVICES IT WAS NOTICES THAT THE TIP OF THE DEVICE AR-8970-03 (LOT: 1392436) IS BROKEN OFF. UPDATE 27-JAN-2026: IT WAS CONFIRMED THAT NO FRAGMENTS REMAINED INSIDE THE PATIENT AND THE DEVICE MIGHT HAVE BROKEN DURING SURGERY.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
314808 T20 HEXALOBE DRIVER MANUAL INSTR, GENERAL SURGICAL MDM ARTHREX, INC. T20 HEXALOBE DRIVER 1392436 00888867133747

Patients

Seq Age Sex Outcome Treatment
1 NA Unknown