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AXSOS 661160Recalls & reported problems

Stryker GmbH · Locking Screw · Class 2 · Implant

All models of AXSOS (184)

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

Adverse event reports
2
Deaths reported
0
Injuries reported
2
Recalls naming it
0

Summary

The FDA's MAUDE database contains 2 adverse event reports that list this exact device (DI 07613252580201), received between Jul 8, 2019 and Jul 8, 2019 — classified as 2 injuries.

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 16, 2026.

Most reported problems

Device problems

  • Adverse Event Without Identified Device or Use Problem1
  • Appropriate Device Problem Term/Code Not Available1

Patient problems

  • Unspecified Infection2

Recent adverse event reports

The 2 most recent of 2 reports, in the reporter's own words as published by the FDA.

  • InjuryJul 8, 2019Appropriate Device Problem Term/Code Not Available

    IT WAS REPORTED THAT ALL HARDWARE IN THE PATIENT'S LEFT FEMUR WAS REMOVED DUE TO INFECTION. SURGEON REPORTED THAT INFECTION OCCURRED AFTER MOLE REMOVAL PERFORMED BY A DERMATOLOGIST. A DLF PLATE AND 11 SCREWS WERE EXPLANTED.

    Patient problems: Unspecified Infection

    MAUDE report 8767110 ↗
  • InjuryJul 8, 2019Adverse Event Without Identified Device or Use Problem

    IT WAS REPORTED THAT ALL HARDWARE IN THE PATIENT'S LEFT FEMUR WAS REMOVED DUE TO INFECTION. SURGEON REPORTED THAT INFECTION OCCURRED AFTER MOLE REMOVAL PERFORMED BY A DERMATOLOGIST. A DLF PLATE AND 11 SCREWS WERE EXPLANTED.

    Patient problems: Unspecified Infection

    MAUDE report 8767103 ↗

Other Plate, fixation, bone devices

All Plate, fixation, bone devices →

Sources and updates

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