MIDAS REX MR8 MR8-9BA40Recalls & reported problems

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 00763000506391), received between Sep 30, 2026 and Sep 30, 2026 — classified as 1 malfunction.

The most frequently reported specific device problem is “Fracture” (1 report).

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 1 most recent of 1 reports, in the reporter's own words as published by the FDA.

• MalfunctionSep 30, 2026Fracture; No Apparent Adverse Event

  It was reported that prior to use, during the initial test performed in the surgery, the attachment malfunctioned, causing the burr to fracture. An intervention was performed and the procedure was completed with backup products, with another attachment and burr used as replacement materials to perform the surgery. At the time of the report, the patient was alive with no injuries.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 50944349 ↗