MIDS REX MR8 MR8-10BA60Recalls & reported problems

Summary

The FDA's MAUDE database contains 2 adverse event reports that list this exact device (DI 00763000487348), received between Nov 19, 2025 and Nov 19, 2025 — classified as 2 malfunctions.

The most frequently reported specific device problem is “Dull, Blunt” (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 2 most recent of 2 reports, in the reporter's own words as published by the FDA.

• MalfunctionNov 19, 2025Overheating of Device; Dull, Blunt; Overheating of Device; Dull, Blunt

  IT WAS REPORTED THAT IN THE SHORT TIME ABOUT 50 SECONDS, BOTH DRILLS WERE NO LONGER ABLE TO MILL THE BONE, AND THEY TENDED TO BURN THE MILLED PART. THERE WAS NO PATIENT INVOLVED WITH THIS EVENT.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 23601286 ↗
• MalfunctionNov 19, 2025Overheating of Device; Dull, Blunt; Overheating of Device; Dull, Blunt

  IT WAS REPORTED THAT IN THE SHORT TIME ABOUT 50 SECONDS, BOTH DRILLS WERE NO LONGER ABLE TO MILL THE BONE, AND THEY TENDED TO BURN THE MILLED PART. THERE WAS NO PATIENT INVOLVED WITH THIS EVENT.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 23601275 ↗