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DISTRACTION, EXTERNAL 51-606-50-91Recalls & reported problems

KLS-Martin L.P. · PIN, DRILL FREE, TI-6AL-4V · Class 2 · Implant

Data updated Oct 18, 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 00888118107992), received between Dec 19, 2019 and Dec 19, 2019 — classified as 1 injury.

The most frequently reported specific device problem is “Loss of Osseointegration” (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

  • Loss of Osseointegration1
  • Use of Device Problem1

Patient problems

  • Impaired Healing1

Recent adverse event reports

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

  • InjuryDec 19, 2019Use of Device Problem; Loss of Osseointegration; Use of Device Problem; Loss of Osseointegration

    IT WAS REPORTED THE DISTRACTOR PIN PULLED FROM THE BONE. THE PINS WERE REMOVED AND REPLACED.

    Patient problems: Impaired Healing

    MAUDE report 9498391 ↗

Other PLATE, BONE devices

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Sources and updates

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