MIDAS REX MR8 MR8-T14BA30Recalls & reported problems

Summary

The FDA's MAUDE database contains 5 adverse event reports that list this exact device (DI 00763000514273), received between Jul 16, 2025 and Jul 16, 2025 — classified as 5 malfunctions.

The most frequently reported specific device problem is “Fracture” (5 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 5 most recent of 5 reports, in the reporter's own words as published by the FDA.

• MalfunctionJul 16, 2025Fracture; Fracture

  IT WAS REPORTED THAT IT BROKE WHILE DRILLING (USE WITH TELESCOPING MR8 ATTACHMENT). IT WAS REPORTED THAT THERE WAS NO PATIENT IMPACT .IT WAS ALSO REPORTED THAT THERE WAS NO INTERVENTION PERFORMED AND THE PROCEDURE GOT COMPLETED WITH BACKUP PRODUCT.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 22517037 ↗
• MalfunctionJul 16, 2025Fracture; Fracture

  IT WAS REPORTED THAT IT BROKE WHILE DRILLING (USE WITH TELESCOPING MR8 ATTACHMENT). IT WAS REPORTED THAT THERE WAS NO PATIENT IMPACT .IT WAS ALSO REPORTED THAT THERE WAS NO INTERVENTION PERFORMED AND THE PROCEDURE GOT COMPLETED WITH BACKUP PRODUCT.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 22517022 ↗
• MalfunctionJul 16, 2025Fracture; Fracture

  IT WAS REPORTED THAT IT BROKE WHILE DRILLING (USE WITH TELESCOPING MR8 ATTACHMENT). IT WAS REPORTED THAT THERE WAS NO PATIENT IMPACT .IT WAS ALSO REPORTED THAT THERE WAS NO INTERVENTION PERFORMED AND THE PROCEDURE GOT COMPLETED WITH BACKUP PRODUCT.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 22517012 ↗
• MalfunctionJul 16, 2025Fracture; Fracture

  IT WAS REPORTED THAT IT BROKE WHILE DRILLING (USE WITH TELESCOPING MR8 ATTACHMENT). IT WAS REPORTED THAT THERE WAS NO PATIENT IMPACT .IT WAS ALSO REPORTED THAT THERE WAS NO INTERVENTION PERFORMED AND THE PROCEDURE GOT COMPLETED WITH BACKUP PRODUCT.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 22516972 ↗
• MalfunctionJul 16, 2025Fracture; Fracture

  IT WAS REPORTED THAT IT BROKE WHILE DRILLING (USE WITH TELESCOPING MR8 ATTACHMENT). IT WAS REPORTED THAT THERE WAS NO PATIENT IMPACT. IT WAS ALSO REPORTED THAT THERE WAS NO INTERVENTION PERFORMED AND THE PROCEDURE GOT COMPLETED WITH BACKUP PRODUCT.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 22516959 ↗