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AXSOS 661475Recalls & reported problems

Stryker GmbH · Cortex Screw · Class 2 · Implant

All models of AXSOS (184)

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 07613252580515), received between Sep 10, 2018 and Sep 10, 2018 — 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 10, 2018Break

    IT WAS REPORTED THAT THE HEADS OF TWO SCREWS TWISTED OFF DURING NORMAL USE. BOTH SCREWHEADS SNAPPED AT THE JUNCTURE OF THE SHAFT THREAD TRANSITION. AS THE SCREWS SNAPPED THEIR HEADS, ADDITIONAL SCREWS HAD TO BE ADDED TO THE PLATE IN ORDER TO COMPENSATE FOR THE LOSS OF FIXATION.

    Patient problems: Failure of Implant

    MAUDE report 7861831 ↗

Other Plate, fixation, bone devices

All Plate, fixation, bone devices →

Sources and updates

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