Arthrex® AR-9094ES-11-3930LRecalls & reported problems

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 00888867412750), received between Oct 22, 2025 and Oct 22, 2025 — classified as 1 malfunction.

The most frequently reported specific device problem is “Use of Device Problem” (1 report).

Reports come from manufacturers, hospitals and patients and are not verified by the FDA. A report does not prove the device caused the event, and counts can't be used to compare devices or estimate failure rates. What reports can and can't tell you · How this data works · Data updated Oct 18, 2026.

Most reported problems

Recent adverse event reports

The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.

• MalfunctionOct 22, 2025Use of Device Problem; Use of Device Problem

  ON 10/17/2025, A SALES REPRESENTATIVE REPORTED VIA (B)(4) THAT A 1268-100 RADIOLUCENT TARGETING ARM, 130 DEGREE TROCH NAIL AND AN AR-9094ES-11-3930L ES TROCHANTERIC NAIL COULD NOT BE USED AS INTENDED. THE ISSUE OCCURRED DURING INSERTION OF THE ES SCREW, WHERE THE SCREW TRAJECTORY WAS INACCURATE, CAUSING IT TO BIND WITHIN THE NAIL. THE SCREW CROSS-THREADED, AND THE SURGEON WAS UNABLE TO FULLY ADVANCE IT THROUGH THE NAIL. THE CASE WAS COMPLETED WITHOUT DISTAL LOCKING OF THE NAIL. ATTEMPTS TO ALIGN THE DRILL ADDED A DELAY OF APPROXIMATELY FIVE TO TEN MINUTES, RESULTING IN AN ADDITIONAL FIVE TO TEN MINUTES OF ANESTHESIA ADMINISTRATION. THE SAME ORIGINAL PART NUMBERS WERE USED TO COMPLETE THE CASE. NO FURTHER INFORMATION IS AVAILABLE. NO PHOTOS WERE TAKEN FOR DOCUMENTATION, AND NO ADVERSE EFFECTS WERE REPORTED. THIS ISSUE WAS IDENTIFIED DURING A HIP FRACTURE PROCEDURE ON (B)(6) 2025, WITH NO REPORTED PATIENT HARM.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 23356435 ↗