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Galaxy UnycoRecalls & reported problems across all models

Orthofix Srl · 4 models in the FDA device registry

Data updated Oct 16, 2026 from official FDA records · Editorial policy

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

We found 4 models of Galaxy Unyco by Orthofix Srl in the FDA's device registry (GUDID). None of them is named in an adverse event report in our data.

1 FDA recall record name at least one of these models by its device 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. Widely used products collect more reports, so totals can't be used to compare products or estimate failure rates. Only reports that name a model's exact device identifier are counted. What reports can and can't tell you · How this data works

Galaxy Unyco recalls

FDA recall records that name at least one of these models by its device identifier, newest first. Each recall usually covers specific models or lots, so check the details.

  1. Jul 5, 2017Terminated

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

    Z-0291-2018 · Root cause: Process change control · names 4 of these models · Recall details · FDA record ↗

Galaxy Unyco models

4 models, most reported first. Each model has its own page with its reports, recalls and device details.

Other Orthofix Srl products

All Orthofix Srl devices →

Sources and updates

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