AOS TROCHANTERIC NAIL 10mm x 20cm x 125° 1030-200Recalls & reported problems

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 00848665014631), received between May 31, 2023 and May 31, 2023 — classified as 1 injury.

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

• InjuryMay 31, 2023Break; Break

  ON 5/5/2023, IT WAS REPORTED BY A SALES REPRESENTATIVE VIA EMAIL THAT A 1030-200 TROCHANTERIC NAIL BROKE ABOUT SIX WEEKS AFTER BEING IMPLANTED. THE SURGEON PERFORMED A REVISION SURGERY AND HAD THE TROCHANTERIC NAIL REMOVED. ADDITIONAL INFORMATION RECEIVED ON 5/5/2023: PER THE SALES REPRESENTATIVE, ON (B)(6) 2022, THE PATIENT UNDERWENT SURGERY IN WHICH A 100MM LAG SCREW, A 5.0MM BY 38MM DISTAL SCREW, AND A 1030-200 TROCHANTERIC NAIL WERE IMPLANTED. AT THE TIME, THE CASE WAS COMPLETED SUCCESSFULLY WITHOUT ANY ISSUES. SIX MONTHS LATER, THE 1030-200 TROCHANTERIC NAIL BROKE, AND THE PATIENT UNDERGOES REVISION SURGERY ON (B)(6) 2023 TO HAVE EVERYTHING REMOVED. THE REVISION SURGERY WAS COMPLETED WITH A LONG NAIL.

  Patient problems: Failure of Implant

  MAUDE report 17029843 ↗