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LEVEL ONE CMF 25-660-07-91Recalls & reported problems

KLS-Martin L.P. · SCREW, CENTREDRIVE, TI-6AL-4V · Class 2 · Implant

All models of LEVEL ONE CMF (150)

Data updated Oct 16, 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 00888118042804), received between Mar 12, 2018 and Mar 12, 2018 — classified as 1 injury.

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 16, 2026.

Most reported problems

Device problems

  • Break1

Patient problems

  • Device Embedded In Tissue or Plaque1

Recent adverse event reports

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

  • InjuryMar 12, 2018Break; Break

    IT WAS REPORTED THAT A SCREW TWISTED/STRIPPED DURING IMPLANTATION. PART OF THE SCREW REMAINS IN THE PATIENT.

    Patient problems: Device Embedded In Tissue or Plaque

    MAUDE report 7330121 ↗

Other PLATE, BONE devices

All PLATE, BONE devices →

Sources and updates

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