MIS MT-RT070Recalls & reported problems

Summary

The FDA's MAUDE database contains 4 adverse event reports that list this exact device (DI 07290109008080), received between Mar 19, 2026 and Jun 25, 2026 — classified as 4 malfunctions.

The most frequently reported specific device problem is “Fracture” (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. How this data works · Data updated Oct 13, 2026.

Most reported problems

Recent adverse event reports

The 4 most recent of 4 reports, in the reporter's own words as published by the FDA.

• MalfunctionJun 25, 2026Fracture

  IT WAS REPORTED THAT THERE WAS A WRENCH ISSUE.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 25620333 ↗
• MalfunctionJun 25, 2026Fracture

  IT WAS REPORTED THAT THERE WAS A TOOL MALFUNCTION WHERE THE TORQUE WRENCH FOR IMPLANT PLACEMENT BROKE DURING USE.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 25618991 ↗
• MalfunctionApr 20, 2026Separation Failure

  CUSTOMER REPORTED THERE WAS A TOOL ISSUE. THE IMPLANT DRIVER PEEK WAS BROKEN.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 24925281 ↗
• MalfunctionMar 19, 2026Mechanical Problem

  CUSTOMER COMPLAINT REGARDING A BROKEN TORQUE WRENCH FOR IMPLANT PLACEMENT.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 24643681 ↗