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Galaxy Unyco 1 (REF 99-93794)Recalls & reported problems

Orthofix Srl · GALAXY UNYCO DIAPHYSEAL TIBIA BOX · Class 2 · Implant

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

Summary

No MAUDE adverse event reports in our data reference this device identifier directly.

1 FDA recall record name this device's identifier.

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. How this data works · Data updated Oct 13, 2026.

Recalls naming this device

  1. Jul 5, 2017Terminated

    The power drill torque limiter may break during use in surgery application.

    Z-0291-2018 · Root cause: Process change control · FDA record ↗

Other Appliance, Fixation, Nail/Blade/Plate Combination, Multiple Component devices

All Appliance, Fixation, Nail/Blade/Plate Combination, Multiple Component devices →

Sources: FDA GUDID, MAUDE and Medical Device Recalls via openFDA. openFDA data is not validated for clinical or regulatory use.