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Midas Rex AA14Recalls & reported problems

Medtronic Powered Surgical Solutions · ATT AA14 LEGEND 14CM ANGLED AM 3.2MM · Class 2

All models of Midas Rex (154)

Data updated Oct 16, 2026 from official FDA records · Editorial policy

Adverse event reports
14
Deaths reported
0
Injuries reported
0
Recalls naming it
0

Summary

The FDA's MAUDE database contains 14 adverse event reports that list this exact device (DI 00763000084615), received between Aug 22, 2022 and Jul 2, 2026 — classified as 14 malfunctions.

The most frequently reported specific device problem is “Overheating of Device” (11 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. What reports can and can't tell you · How this data works · Data updated Oct 16, 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: 3 reportsMar 2025: 4 reportsApr 2025: 0 reportsMay 2025: 0 reportsJun 2025: 0 reportsJul 2025: 0 reportsAug 2025: 1 reportsSep 2025: 0 reportsOct 2025: 1 reportsNov 2025: 0 reportsDec 2025: 0 reportsJan 2026: 0 reportsFeb 2026: 0 reportsMar 2026: 0 reportsApr 2026: 0 reportsMay 2026: 0 reportsJun 2026: 3 reportsJul 2026: 1 reportsAug 2026: 0 reportsSep 2026: 0 reportsOct 2026: 0 reports2024202520264
Last 36 months. The most recent month may be incomplete.

Most reported problems

Device problems

  • Overheating of Device11
  • Difficult to Insert2
  • No Apparent Adverse Event1

Patient problems

  • No Clinical Signs, Symptoms or Conditions14

Recent adverse event reports

The 14 most recent of 14 reports, in the reporter's own words as published by the FDA.

  • MalfunctionJul 2, 2026No Apparent Adverse Event

    IT WAS REPORTED THAT CUSTOMER HAD A DISSATISFACTION WITH THE ATTACHMENT. IT WAS REPORTED THAT THERE WAS NO PATIENT OR STAFF IMPACT. ADDITIONAL INFORMATION WAS RECEIVED STATING THAT BEARINGS WERE DETACHED FOUND IN ANALYSIS.

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 25695557 ↗
  • MalfunctionJun 19, 2026Overheating of Device

    IT WAS REPORTED THAT PRIOR TO USE, A HEATING ISSUE WAS OBSERVED WITH THE ATTACHMENT DURING PRE-OPERATIVE PREPARATION. IT WAS REPORTED THAT THERE WAS NO PATIENT INVOLVEMENT.

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 25557107 ↗
  • MalfunctionJun 5, 2026Difficult to Insert

    IT WAS REPORTED THAT THE TOOL CANNOT BE INSERTED PRIOR TO USE. IT WAS REPORTED THAT THERE WAS NO PATIENT INVOLVEMENT. ADDITIONAL INFORMATION WAS RECEIVED STATING THAT BEARING FRACTURE WERE FOUND DURING EVALUATION.

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 25406660 ↗
  • MalfunctionJun 4, 2026Difficult to Insert

    IT WAS REPORTED THAT DURING PRE OPERATIVELY, BLADE CANNOT BE INSERTED. AT THE TIME OF REPORT, THERE WAS NO PATIENT INVOLVEMENT.

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 25403255 ↗
  • MalfunctionOct 16, 2025Overheating of Device; Overheating of Device

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

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 23308058 ↗
  • MalfunctionAug 5, 2025Overheating of Device; Overheating of Device

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

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 22713235 ↗
  • MalfunctionMar 21, 2025Overheating of Device; Overheating of Device

    REPAIR REQUEST INITIATED FOR DEVICE WITH THE REPORT OF OVERHEATING. IT WAS REPORTED THERE WAS NO PATIENT INVOLVEMENT.

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 21661645 ↗
  • MalfunctionMar 14, 2025Overheating of Device; Overheating of Device

    REPAIR REQUEST INITIATED FOR DEVICE WITH THE REPORT OF OVERHEATING. IT WAS REPORTED THERE WAS NO PATIENT INVOLVEMENT.

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 21603034 ↗
  • MalfunctionMar 12, 2025Overheating of Device; Overheating of Device

    REPAIR REQUEST INITIATED FOR DEVICE WITH THE REPORT OF OVERHEATING. IT WAS REPORTED THERE WAS NO PATIENT INVOLVEMENT.

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 21581561 ↗
  • MalfunctionMar 10, 2025Overheating of Device; Overheating of Device

    REPAIR REQUEST INITIATED FOR DEVICE WITH THE REPORT OF OVERHEATING. IT WAS REPORTED THERE WAS NO PATIENT INVOLVEMENT.

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 21558943 ↗
  • MalfunctionFeb 19, 2025Overheating of Device; Overheating of Device

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

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 21414735 ↗
  • MalfunctionFeb 19, 2025Overheating of Device; Overheating of Device

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

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 21409122 ↗
  • MalfunctionFeb 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 INVOLVEMENT.

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 21393751 ↗
  • MalfunctionAug 22, 2022Overheating of Device; Overheating of Device

    REPAIR REQUEST INITIATED FOR DEVICE WITH THE REPORT OF OVERHEATING. IT WAS REPORTED THAT THERE WAS NO PATIENT INVOLVEMENT. REPAIR REQUEST ESCALATED TO A PRODUCT EVENT BASED ON REASON FOR RETURN.

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 15265429 ↗

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Sources and updates

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