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EasyDrill Cranial Perforator Ø9 x Ø6 x 3mm DM0008FAA (UDI 07898959543326)Recalls & reported problems

Micromar Indústria e Comércio Ltda · Class 2

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 07898959543326), received between Oct 9, 2020 and Oct 9, 2020 — classified as 1 malfunction.

The most frequently reported specific device problem is “Device Remains Activated” (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

  • Device Remains Activated1

Patient problems

  • No Clinical Signs, Symptoms or Conditions1
  • No Consequences Or Impact To Patient1

Recent adverse event reports

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

  • MalfunctionOct 9, 2020Device Remains Activated; Device Remains Activated

    ON FOLLOW-UP, IT WAS CONFIRMED THAT THE DRILL DID NOT STOP.

    Patient problems: No Clinical Signs, Symptoms or Conditions; No Consequences Or Impact To Patient

    MAUDE report 10659008 ↗

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Sources and updates

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