MIS MT-LRH20Recalls & reported problems

Summary

The FDA's MAUDE database contains 3 adverse event reports that list this exact device (DI 07290109006802), received between Mar 18, 2026 and Sep 24, 2026 — classified as 3 malfunctions.

The most frequently reported specific device problem is “Mechanical Problem” (3 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 3 most recent of 3 reports, in the reporter's own words as published by the FDA.

• MalfunctionSep 24, 2026Mechanical Problem

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 50881860 ↗
• MalfunctionJun 11, 2026Mechanical Problem

  IT WAS REPORTED THAT ITS NOT ENGAGING THE IMPLANT PROPERLY AND IMPLANTS KEEP FALLING OFF.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 25467558 ↗
• MalfunctionMar 18, 2026Mechanical Problem

  IT WAS REPORTED THAT THE INSERTION TOOL COULD NOT HOLD THE IMPLANT.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 24628373 ↗