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AOS ES™ TROCHANTERIC NAIL, LEFT 11mm x 42cm x 130° 1058-425Recalls & reported problems

Advanced Orthopaedic Solutions, Inc. · Class 2 · Implant

Data updated Oct 18, 2026 from official FDA records · Editorial policy

Adverse event reports
1
Deaths reported
0
Injuries reported
0
Recalls naming it
0

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 00848665015188), received between Sep 19, 2022 and Sep 19, 2022 — classified as 1 malfunction.

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

Device problems

  • Break1

Patient problems

  • Failure of Implant1

Recent adverse event reports

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

  • MalfunctionSep 19, 2022Break

    IT WAS REPORTED ON 09/01/2022 BY A SALES REPRESENTATIVE VIA EMAIL THAT AN 1058-425 TROCHANTERIC NAIL BROKE AT THE LAG SCREW HOLE AND HAD TO BE REMOVED THROUGH A REVISION SURGERY. THIS WAS REPLACED WITH A NEW NAIL.

    Patient problems: Failure of Implant

    MAUDE report 15445796 ↗

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Sources and updates

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