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Midas RexRecalls & reported problems across all models

Medtronic Powered Surgical Solutions · 154 models in the FDA device registry

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

Adverse event reports
1,518
Deaths reported
0
Injuries reported
106
Recalls
0

We found 154 models of Midas Rex by Medtronic Powered Surgical Solutions in the FDA's device registry (GUDID). Together they are named in 1,518 adverse event reports in the FDA's MAUDE database, received between Jan 31, 2017 and Sep 29, 2026 — classified as 106 injuries, 1,412 malfunctions.

The most frequently reported specific device problem is “Overheating of Device” (745 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: 4 reportsDec 2023: 12 reportsJan 2024: 6 reportsFeb 2024: 7 reportsMar 2024: 6 reportsApr 2024: 5 reportsMay 2024: 3 reportsJun 2024: 1 reportsJul 2024: 4 reportsAug 2024: 43 reportsSep 2024: 67 reportsOct 2024: 20 reportsNov 2024: 9 reportsDec 2024: 5 reportsJan 2025: 11 reportsFeb 2025: 186 reportsMar 2025: 131 reportsApr 2025: 27 reportsMay 2025: 12 reportsJun 2025: 10 reportsJul 2025: 13 reportsAug 2025: 9 reportsSep 2025: 3 reportsOct 2025: 2 reportsNov 2025: 6 reportsDec 2025: 4 reportsJan 2026: 0 reportsFeb 2026: 0 reportsMar 2026: 11 reportsApr 2026: 18 reportsMay 2026: 73 reportsJun 2026: 155 reportsJul 2026: 31 reportsAug 2026: 7 reportsSep 2026: 8 reportsOct 2026: 0 reports202420252026186
Last 36 months. The most recent month may be incomplete.

Most reported Midas Rex problems

Device problems

  • Overheating of Device745
  • Detachment of Device or Device Component232
  • No Apparent Adverse Event182
  • Material Puncture/Hole150
  • Naturally Worn112
  • Difficult to Insert103
  • Fracture68
  • Noise, Audible53

Patient problems

  • No Clinical Signs, Symptoms or Conditions1,274
  • No Consequences Or Impact To Patient100
  • No Patient Involvement38
  • Insufficient Information27
  • No Known Impact Or Consequence To Patient23
  • Chemical Exposure19
  • Burn(s)18
  • Perforation17

Midas Rex models

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

Recent Midas Rex 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