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EasyDrill Cranial Perforator Ø11 x Ø7 x 3mm DM0011FAA (UDI 07898959543067)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
1
Recalls naming it
0

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 07898959543067), received between Sep 11, 2019 and Sep 11, 2019 — classified as 1 injury.

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

  • Perforation1

Recent adverse event reports

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

  • InjurySep 11, 2019Device Remains Activated; Device Remains Activated

    ADDITIONAL INFORMATION RECEIVED THAT AN AD03 ATTACHMENT WAS USED TOGETHER WITH THE PERFORATOR.

    Patient problems: Perforation

    MAUDE report 8998255 ↗

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Sources and updates

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