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PHOENIX NAIL SYSTEM 14-405050Recalls & reported problems

Biomet Orthopedics, LLC · Class 2

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

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

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 00887868092626), received between Jul 9, 2021 and Jul 9, 2021 — classified as 1 injury.

5 other recalls cover devices cleared under the same FDA submission (K050118, K063570); they may or may not involve this specific model.

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

  • Adverse Event Without Identified Device or Use Problem1

Patient problems

  • Pain1

Recent adverse event reports

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

  • InjuryJul 9, 2021Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem

    T WAS REPORTED THAT THE PATIENT UNDERWENT A REVISION PROCEDURE APPROXIMATELY EIGHTEEN MONTHS POST INITIAL SURGERY DUE TO KNEE PAIN. NO ADDITIONAL PATIENT CONSEQUENCES WERE REPORTED. IT WAS INDICATED THAT THE PAIN WAS NOT RELATED TO THE IMPLANT, IT WAS ALLEGED ON INSTRUMENTATION AND UNCERTAIN IF IT IS RELATED TO THE PROCEDURE. NO ADDITIONAL INFORMATION WAS PROVIDED.

    Patient problems: Pain

    MAUDE report 12146135 ↗

Recalls under the same FDA submission

These recalls involve devices cleared under K050118, K063570. One submission often covers many models, so check the product and lot details in each record.

  • Z-0625-2021 · Nov 25, 2020 · Terminated
    PHOENIX, Interlocking screw for IM nail, Item numbers 14-405040, 14-405042, 14-405044, 14-405070 - Product Usage: Fracture fixation of small bones, small bone fragements and long b
  • Z-0627-2021 · Nov 25, 2020 · Terminated
    RINGLOC ACETABULAR SYSTEM Self-tapping bone screws, Item numbers 103531, 103533, 103534, 103535 - Product Usage: Prosthesis, Hip, Semi-Constrained, Metal/Polymer, Cemented; Prosthe
  • Z-1819-2016 · Apr 1, 2016 · Terminated
    Various trauma and sports medicine instruments and implants. Rod, fixation, intramedullary and accessories.
  • Z-1478-2012 · Mar 30, 2012 · Terminated
    REF 28234 Troch Nail, Long 11MM, Right 34 CM Peritrochanteric Nail System, Rx Sterile Biomet Trauma Persippany, NJ Rod, Fixation, Intramedullary and Accessories Product Usage: An
  • Z-0012-06 · Jun 24, 2005 · Terminated
    EBI Trochanteric 11mm Long Nail.

Other ROD, FIXATION, INTRAMEDULLARY AND ACCESSORIES devices

All ROD, FIXATION, INTRAMEDULLARY AND ACCESSORIES devices →

Sources and updates

How reports and recalls are matched · Editorial policy · Report an error on this page