FDA Adverse Event Malfunction Summary report: N

STRAIGHT PLATE, 1.4MM, 10 HOLE

MDR report key: 24344277 · Received February 16, 2026

Report

Report Number
1220246-2026-00600
Event Type
Malfunction
Date Received
February 16, 2026
Date of Event
January 28, 2026
Report Date
February 16, 2026
Manufacturer
ARTHREX, INC.
Product Code
HRS
UDI-DI
00888867315556
PMA / PMN Number
K191326
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
DE, US
Reporter Occupation
501

Narratives

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) 2026, A SALES REPRESENTATIVE REPORTED VIA EMAIL THAT AN AR-18714-12 CORTICAL SCREW (1.4 MM × 12 MM) EXPERIENCED A HEAD FRACTURE DURING INSERTION. THE SCREW WAS BEING PLACED INTO A HOLE OF A 10-HOLE 1.4 MM PLATE AND HAD BEEN ADVANCED NEARLY FLUSH TO THE PLATE WHEN THE HEAD SEPARATED FROM THE SHAFT. THE SURGEON REMOVED ONLY THE SCREW HEAD, LEAVING THE SCREW SHAFT IN SITU BECAUSE IT CROSSED THE FRACTURE SITE. THE EVENT OCCURRED DURING A METACARPAL FRACTURE INTERNAL FIXATION PROCEDURE ON (B)(6) 2026. THE ISSUE DID NOT CAUSE PROCEDURAL DELAY, AND NO PATIENT HARM WAS REPORTED. ADDITIONAL INFORMATION WAS RECEIVED ON 03-FEB-2026: THERE WAS NO REPORTED DAMAGE TO THE AR-18714P-07 STRAIGHT PLATE, 1.4 MM, 10-HOLE ASSOCIATED WITH THIS EVENT. THE ONLY ISSUE IDENTIFIED INVOLVED A SINGLE AR-18714-12 CORTICAL SCREW (1.4 MM × 12 MM), AS SHOWN IN THE ATTACHED PHOTO. THE PROCEDURE WAS COMPLETED SUCCESSFULLY, AND THE AFFECTED SCREW REMAINED IMPLANTED. ADDITIONAL SCREWS MEASURING 10 MM, 11 MM, 12 MM, AND 15 MM IN LENGTH WERE ALSO UTILIZED AS PART OF THE CONSTRUCT. NO ADVERSE PATIENT EFFECTS WERE REPORTED IN RELATION TO THIS ISSUE.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
404423 STRAIGHT PLATE, 1.4MM, 10 HOLE BONE FIXATION SCREW/PLATE HRS ARTHREX, INC. STRAIGHT PLATE, 1.4MM, 10 HOLE UNK 00888867315556

Patients

Seq Age Sex Outcome Treatment
1 NA Unknown