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Dermatome 00-8821-006-00Recalls & reported problems

Zimmer Orthopaedic Surgical Products, Inc. · Electric Dermatome Power Supply · Class 1

All models of Dermatome (5)

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 00889024376007), received between Feb 28, 2022 and Feb 28, 2022 — classified as 1 malfunction.

The most frequently reported specific device problem is “Material Frayed” (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

  • Material Frayed1
  • Mechanical Problem1

Patient problems

  • No Clinical Signs, Symptoms or Conditions1

Recent adverse event reports

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

  • MalfunctionFeb 28, 2022Material Frayed; Mechanical Problem; Material Frayed; Mechanical Problem

    IT WAS REPORTED THE UNIT HAD A FRAYED POWER CORD. THERE WAS NO HARM OR DELAY REPORTED. NO ADVERSE EVENTS WERE REPORTED AS A RESULT OF THIS MALFUNCTION

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 13623190 ↗

Other Dermatome devices

All Dermatome devices →

Sources and updates

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