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MIDAS REX MR8 EM810 (UDI 00763000430931)Recalls & reported problems

Medtronic Powered Surgical Solutions · MOTOR EM810 MR8 ELECTRIC TOUCH · Class 2

Adverse event reports
7
Deaths reported
0
Injuries reported
0
Recalls naming it
0

Summary

The FDA's MAUDE database contains 7 adverse event reports that list this exact device (DI 00763000430931), received between Feb 24, 2025 and Dec 23, 2025 — classified as 7 malfunctions.

The most frequently reported specific device problem is “Overheating of Device” (4 reports).

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. How this data works · Data updated Oct 13, 2026.

Reports received per month

Nov 2023: 0 reportsDec 2023: 0 reportsJan 2024: 0 reportsFeb 2024: 0 reportsMar 2024: 0 reportsApr 2024: 0 reportsMay 2024: 0 reportsJun 2024: 0 reportsJul 2024: 0 reportsAug 2024: 0 reportsSep 2024: 0 reportsOct 2024: 0 reportsNov 2024: 0 reportsDec 2024: 0 reportsJan 2025: 0 reportsFeb 2025: 1 reportsMar 2025: 2 reportsApr 2025: 1 reportsMay 2025: 0 reportsJun 2025: 0 reportsJul 2025: 1 reportsAug 2025: 0 reportsSep 2025: 0 reportsOct 2025: 0 reportsNov 2025: 1 reportsDec 2025: 1 reportsJan 2026: 0 reportsFeb 2026: 0 reportsMar 2026: 0 reportsApr 2026: 0 reportsMay 2026: 0 reportsJun 2026: 0 reportsJul 2026: 0 reportsAug 2026: 0 reportsSep 2026: 0 reportsOct 2026: 0 reports2024202520262
Last 36 months. The most recent month may be incomplete.

Most reported problems

Device problems

  • Overheating of Device4
  • Corroded2
  • Device Remains Activated1

Patient problems

  • No Clinical Signs, Symptoms or Conditions7

Recent adverse event reports

The 7 most recent of 7 reports, in the reporter's own words as published by the FDA.

  • MalfunctionDec 23, 2025Device Remains Activated; Device Remains Activated

    IT WAS REPORTED THAT THE MOTOR CONTINUED TO RUN AND DID NOT TURN OFF PROPERLY PRIOR TO USE IN A PRE-OPERATIVE SETTING. IT WAS REPORTED THAT THERE WAS NO PATIENT IMPACT.

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 23875130 ↗
  • MalfunctionNov 28, 2025Corroded; Corroded

    IT WAS REPORTED THAT MOTOR WAS CORRODED. IT WAS REPORTED THAT THERE WAS NO PATIENT IMPACT. ADDITIONAL INFORMATION WAS RECEIVED STATING THAT DEVICE WAS OVERHEATING.

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 23673918 ↗
  • MalfunctionJul 29, 2025Corroded; Corroded

    REPAIR REQUEST INITIATED FOR DEVICE WITH THE REPORT OF CORROSION. IT WAS REPORTED THAT THERE WAS NO PATIENT IMPACT.

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 22640742 ↗
  • MalfunctionApr 3, 2025Overheating of Device; Overheating of Device

    REPAIR REQUEST INITIATED FOR DEVICE WITH THE REPORT OF OVERHEATING. NO PATIENT IMPACT REPORTED.

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 21763118 ↗
  • MalfunctionMar 18, 2025Overheating of Device; Overheating of Device

    REPAIR REQUEST INITIATED FOR DEVICE WITH THE REPORT OF OVERHEATING. IT WAS REPORTED THAT THERE WAS NO PATIENT OR STAFF IMPACT.

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 21629102 ↗
  • MalfunctionMar 13, 2025Overheating of Device; Overheating of Device

    REPAIR REQUEST INITIATED FOR DEVICE WITH THE REPORT OF OVERHEATING. IT WAS REPORTED THAT THERE WAS NO PATIENT OR STAFF IMPACT.

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 21591104 ↗
  • MalfunctionFeb 24, 2025Overheating of Device; Overheating of Device

    REPAIR REQUEST INITIATED FOR DEVICE WITH THE REPORT OF OVERHEATING. NO PATIENT IMPACT REPORTED. ON FOLLOW-UP IT WAS REPORTED THAT THERE WAS NO PATIENT OR STAFF IMPACT.

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 21449587 ↗

Other MOTOR, DRILL, ELECTRIC devices

All MOTOR, DRILL, ELECTRIC devices →

Sources: FDA GUDID, MAUDE and Medical Device Recalls via openFDA. openFDA data is not validated for clinical or regulatory use.