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Midas Rex MR8 MR8-14MH30 (UDI 00643169844322)Recalls & reported problems

Medtronic Powered Surgical Solutions · TOOL MR8-14MH30 MR8 14CM MATCH 3MM · Class 1

All models of MIDAS REX MR8 (137)

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 00643169844322), received between Apr 9, 2021 and Apr 9, 2021 — classified as 1 injury.

The most frequently reported specific device problem is “Dull, Blunt” (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

  • Dull, Blunt1

Patient problems

  • Burn(s)1
  • 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.

  • InjuryApr 9, 2021Dull, Blunt; Dull, Blunt

    ON FOLLOW-UP, IT WAS CONFIRMED THAT THERE WAS NO PATIENT IMPACT AND THERE WAS NO ADDITIONAL INTERVENTIONS PERFORMED BECAUSE OF THE EVENT.

    Patient problems: Burn(s); No Clinical Signs, Symptoms or Conditions

    MAUDE report 11642305 ↗

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Sources and updates

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