Arthrex® AR-9094-10-2030Recalls & reported problems

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 00888867411548), received between Jun 7, 2024 and Jun 7, 2024 — 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.

• MalfunctionJun 7, 2024Use of Device Problem; Use of Device Problem

  ON 05/09/2024, IT WAS REPORTED BY A SALES REPRESENTATIVE VIA EMAIL THAT AN 1192-100 TELESCOPING LAG SCREW, A 1099-110 TELESCOPING LAG SCREW, AND A 1099-100 TELESCOPING LAG SCREW WOULD NOT ADVANCE INTO THE FEMORAL HEAD OF AN AR-9094-10-2030 TROCHANTERIC NAIL. THE TELESCOPING LAG SCREWS WERE USED WITH A NEW TROCHANTERIC NAIL; HOWEVER, THE ISSUE PERSISTED, AND THE TELESCOPING LAG SCREWS WOULD STILL NOT ADVANCE. THE CASE WAS COMPLETED USING A NEW TROCHANTERIC NAIL AND A NEW 1099-110 TELESCOPING LAG SCREW. THE CASE WAS DELAYED ABOUT FIFTEEN MINUTES. THIS WAS DISCOVERED DURING A LEFT HIP IM NAIL PROCEDURE ON (B)(6) 2024.

  Patient problems: Insufficient Information

  MAUDE report 19487721 ↗