MIDAS REX MR8 MR8-T14MH25TRecalls & reported problems

Summary

The FDA's MAUDE database contains 2 adverse event reports that list this exact device (DI 00763000514334), received between Jan 20, 2026 and Jan 20, 2026 — 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 18, 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.

• MalfunctionJan 20, 2026Fracture; Dull, Blunt

  IT WAS REPORTED THAT DURING THE PROCEDURE THE TWO DRILL BIT WAS BROKEN AND DULL AND ONE DRILL BIT WAS DULL. AT THE TIME OF THE REPORT, THERE WAS NO PATIENT IMPACT. THE PROCEDURE WAS COMPLETED WITH BACKUP PRODUCTS AND THERE WAS NO DELAY IN THE PROCEDURE. IT WAS ALSO REPORTED THAT THERE WAS INTERVENTION PERFORMED, NO DAMAGED PIECE REMAINED IN THE PATIENT'S BODY.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 24112557 ↗
• MalfunctionJan 20, 2026Fracture; Dull, Blunt

  IT WAS REPORTED THAT DURING THE PROCEDURE THE TWO DRILL BIT WAS BROKEN AND DULL AND ONE DRILL BIT WAS DULL. AT THE TIME OF THE REPORT, THERE WAS NO PATIENT IMPACT. THE PROCEDURE WAS COMPLETED WITH BACKUP PRODUCTS AND THERE WAS NO DELAY IN THE PROCEDURE. IT WAS ALSO REPORTED THAT THERE WAS INTERVENTION PERFORMED, NO DAMAGED PIECE REMAINED IN THE PATIENT'S BODY. ADDITIONAL INFORMATION REGARDING THE PATIENT IMPACT WAS BEING FOLLOWED UP FROM THE FACILITY.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 24112550 ↗