Arthrex® AR-9094-085LRecalls & reported problems

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 00888867409989), received between Feb 2, 2026 and Feb 2, 2026 — classified as 1 malfunction.

The most frequently reported specific device problem is “Positioning Failure” (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.

• MalfunctionFeb 2, 2026Positioning Failure

  ON 08-JAN-2026, IT WAS REPORTED BY A SALES REPRESENTATIVE VIA PHONE THAT AN AR-9094-090L LEFT LAG SCREW, AN AR-S0100-381 GUIDE PIN, AN AR-S0457-000 ACTIVATION TOOL, AR-S0100-000 GUIDE PIN, AR-S0219-100 DRILL, AR-S0209-200 DRILL, AR-9094-11-2030 TROCHANTERIC NAIL, AND AN AR-9094-085L LAG SCREW WERE USED IN A CASE AND NEITHER SCREW WERE ABLE TO LOCK INTO THE NAIL AFTER IMPLANTATION. ALL IMPLANTS WERE FULLY EXPLANTED, AND THE SURGERY WAS COMPLETED USING A COMPETITOR PRODUCT NAIL. THIS OCCURRED DURING USE IN A CASE WITH NO PATIENT EFFECT. DELAY IN CASE 50 MINUTES.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 24234138 ↗