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MIDAS REX MR8Recalls & reported problems across all models

Medtronic Powered Surgical Solutions · 137 models in the FDA device registry

Data updated Oct 18, 2026 from official FDA records · Editorial policy

Adverse event reports
3,685
Deaths reported
0
Injuries reported
39
Recalls
0

We found 137 models of MIDAS REX MR8 by Medtronic Powered Surgical Solutions in the FDA's device registry (GUDID). Together they are named in 3,685 adverse event reports in the FDA's MAUDE database, received between Nov 9, 2020 and Sep 30, 2026 — classified as 39 injuries, 3,646 malfunctions.

The most frequently reported specific device problem is “Overheating of Device” (877 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. Widely used products collect more reports, so totals can't be used to compare products or estimate failure rates. Only reports that name a model's exact device identifier are counted. What reports can and can't tell you · How this data works

Reports received per month, all models

Nov 2023: 6 reportsDec 2023: 8 reportsJan 2024: 5 reportsFeb 2024: 8 reportsMar 2024: 8 reportsApr 2024: 9 reportsMay 2024: 4 reportsJun 2024: 6 reportsJul 2024: 10 reportsAug 2024: 65 reportsSep 2024: 199 reportsOct 2024: 28 reportsNov 2024: 34 reportsDec 2024: 36 reportsJan 2025: 33 reportsFeb 2025: 53 reportsMar 2025: 117 reportsApr 2025: 31 reportsMay 2025: 26 reportsJun 2025: 32 reportsJul 2025: 56 reportsAug 2025: 33 reportsSep 2025: 40 reportsOct 2025: 25 reportsNov 2025: 46 reportsDec 2025: 29 reportsJan 2026: 7 reportsFeb 2026: 36 reportsMar 2026: 190 reportsApr 2026: 342 reportsMay 2026: 324 reportsJun 2026: 1,199 reportsJul 2026: 245 reportsAug 2026: 68 reportsSep 2026: 243 reportsOct 2026: 0 reports2024202520261,199
Last 36 months. The most recent month may be incomplete.

Most reported MIDAS REX MR8 problems

Device problems

  • Overheating of Device877
  • No Apparent Adverse Event838
  • Detachment of Device or Device Component781
  • Naturally Worn543
  • Difficult to Insert307
  • Loss of Power149
  • Difficult to Remove131
  • Vibration114

Patient problems

  • No Clinical Signs, Symptoms or Conditions3,453
  • Insufficient Information231
  • Unintended Radiation Exposure18
  • Burn(s)12
  • Device Embedded In Tissue or Plaque9
  • Dural Tear2
  • Perforation2
  • Spinal Cord Injury2

MIDAS REX MR8 models

137 models, 100 per page, most reported first. Each model has its own page with its reports, recalls and device details.

Recent MIDAS REX MR8 adverse event reports

The 15 most recent reports across all models, in the reporter's own words as published by the FDA.

Other Medtronic Powered Surgical Solutions products

All Medtronic Powered Surgical Solutions devices →

Sources and updates

How reports and recalls are matched · Editorial policy · Report an error on this page