Midas Rex AA075Recalls & reported problems
Medtronic Powered Surgical Solutions · ATT AA075 LEGEND 7.5CM ANGLED 2.4MM · Class 2
All models of Midas Rex (154)
Data updated Oct 16, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 5
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 5 adverse event reports that list this exact device (DI 00763000084530), received between Mar 9, 2022 and Jun 15, 2026 — classified as 5 malfunctions.
The most frequently reported specific device problem is “Overheating of Device” (3 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
Most reported problems
Device problems
- Overheating of Device3
- No Apparent Adverse Event1
- Physical Resistance/Sticking1
- Vibration1
Patient problems
- No Clinical Signs, Symptoms or Conditions5
Recent adverse event reports
The 5 most recent of 5 reports, in the reporter's own words as published by the FDA.
MalfunctionJun 15, 2026Overheating of Device
IT WAS REPORTED THAT DURING PREOP, ATTACHMENT HAS HEATING ISSUE. IT WAS REPORTED THAT THERE WAS NO PATIENT OR STAFF IMPACT.ADDITIONAL INFORMATION WAS RECEIVED STATING THAT THERE WERE DETACHED BEARINGS INSIDE THE DEVICE
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 25501181 ↗MalfunctionJun 1, 2026Overheating of Device
IT WAS REPORTED THAT PRIOR TO USE, ATTACHMENT HAD HEATING PROBLEM. IT WAS REPORTED THAT THERE WAS NO PATIENT INVOLVEMENT.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 25348918 ↗MalfunctionMar 31, 2026Physical Resistance/Sticking
IT WAS REPORTED THAT THE DEVICE BUR MECHANISM GOT JAMMED. IT WAS REPORTED THAT THERE WAS NO PATIENT INVOLVEMENT.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 24739437 ↗MalfunctionSep 25, 2024Vibration; Vibration
REPAIR REQUEST INITIATED FOR DEVICE WITH THE REPORT OF WOBBLING. NO PATIENT IMPACT REPORTED. REPAIR REQUEST ESCALATED TO A PRODUCT EVENT BASED ON REASON FOR RETURN.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 20298839 ↗MalfunctionMar 9, 2022Overheating of Device; No Apparent Adverse Event; Overheating of Device; No Apparent Adverse Event
REPAIR REQUEST INITIATED FOR DEVICE WITH NO REPORTED MALFUNCTION. IT WAS REPORTED THAT THERE WAS NO PATIENT OR STAFF IMPACT. REPAIR ESCALATED TO PRODUCT EVENT ON EVALUATION DUE TO OVERHEATING.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 13708607 ↗
Other MOTOR, DRILL, PNEUMATIC devices
- NA 05.001.080Synthes GmbH · MOTOR, DRILL, PNEUMATIC432 reports
- NA CSR60Synthes GmbH · MOTOR, DRILL, PNEUMATIC221 reports
- Midas Rex® AF02Medtronic Powered Surgical Solutions · MOTOR, DRILL, PNEUMATIC163 reports
- Maestro Air 5407-200-000Stryker Corporation · MOTOR, DRILL, PNEUMATIC112 reports
- Maestro 5400210060Stryker Corporation · MOTOR, DRILL, PNEUMATIC95 reports
- MIDAS REX™ AF02Medtronic Powered Surgical Solutions · MOTOR, DRILL, PNEUMATIC91 reports
- CORE, Maestro 5400200000Stryker Corporation · MOTOR, DRILL, PNEUMATIC75 reports
- Maestro Air 5407-200-00HStryker Corporation · MOTOR, DRILL, PNEUMATIC56 reports
Sources and updates
- Device record: FDA GUDID, file dated Oct 13, 2026 · View this device in AccessGUDID ↗
- Adverse event reports: FDA MAUDE, file dated Oct 14, 2026 · each report above links to its original FDA record
- Recalls: FDA Medical Device Recalls, file dated Oct 16, 2026
- Page last rebuilt: Oct 16, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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