Skip to content

LEVEL ONE CMF 25-550-04-91Recalls & reported problems

KLS-Martin L.P. · PLATE, MINI, STR, 2.0 MM SCREW, CP TITANIUM · Class 2 · Implant

All models of LEVEL ONE CMF (150)

Data updated Oct 18, 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 00888118042040), received between Jul 20, 2018 and Nov 4, 2019 — classified as 2 injuries.

The most frequently reported specific device problem is “Device Dislodged or Dislocated” (2 reports).

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

  • Device Dislodged or Dislocated2
  • Break1

Patient problems

  • Impaired Healing2

Recent adverse event reports

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

  • InjuryNov 4, 2019Break; Device Dislodged or Dislocated; Break; Device Dislodged or Dislocated

    IT WAS REPORTED THAT THE PLATE WAS DISLODGED OR BROKEN. THE PLATE IS EXPECTED TO BE REMOVED ON AN UNKNOWN DATE.

    Patient problems: Impaired Healing

    MAUDE report 9271264 ↗
  • InjuryJul 20, 2018Device Dislodged or Dislocated; Device Dislodged or Dislocated

    IT WAS REPORTED A SCREW AND PLATE PULLED OUT OF THE BONE, DEVICES WERE REMOVED AND REPLACED.

    Patient problems: Impaired Healing

    MAUDE report 7706954 ↗

Other PLATE, BONE devices

All PLATE, BONE devices →

Sources and updates

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