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Midas Rex MR8 EA815 (UDI 00763000374785)Recalls & reported problems

Medtronic Ps Medical, Inc. · ACCY EA815 MR8 ELECTRIC CONTROL SWITCH · Class 2

All models of Midas Rex MR8 (41)

Data updated Oct 16, 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 00763000374785), received between May 18, 2023 and May 18, 2023 — classified as 1 malfunction.

The most frequently reported specific device problem is “Detachment of Device or Device Component” (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 16, 2026.

Most reported problems

Device problems

  • Detachment of Device or Device Component1

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.

  • MalfunctionMay 18, 2023Detachment of Device or Device Component; Detachment of Device or Device Component

    REPAIR REQUEST INITIATED FOR DEVICE WITH REPORT OF PARTS DETACHED. IT WAS REPORTED THAT THERE WAS NO PATIENT IMPACT. REPAIR REQUEST ESCALATED TO A PRODUCT EVENT DUE REASON FOR RETURN.

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 16951017 ↗

Other DRILLS, BURRS, TREPHINES & ACCESSORIES (SIMPLE, POWERED) devices

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Sources and updates

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