MIDAS REX MR8 MR8-AA09DK (UDI 00763000440831)Recalls & reported problems

Summary

The FDA's MAUDE database contains 3 adverse event reports that list this exact device (DI 00763000440831), received between Jun 5, 2026 and Sep 23, 2026 — classified as 3 malfunctions.

The most frequently reported specific device problem is “Overheating of Device” (2 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.

Most reported problems

Recent adverse event reports

The 3 most recent of 3 reports, in the reporter's own words as published by the FDA.

• MalfunctionSep 23, 2026Overheating of Device

  It was reported that during pre op, the attachment was overheating.  It was reported that there was no patient impact.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 50867348 ↗
• MalfunctionSep 23, 2026No Apparent Adverse Event

  Patient problems: Insufficient Information

  MAUDE report 50865495 ↗
• MalfunctionJun 5, 2026Corroded; Overheating of Device

  IT WAS REPORTED THAT ATTACHMENT WAS OVERHEATING AND HAD CORROSION. AT THE TIME OF REPORT, THERE WAS NO KNOWN IMPACT TO A PATIENT.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 25404034 ↗