MIS MT-CD310Recalls & reported problems

Summary

The FDA's MAUDE database contains 2 adverse event reports that list this exact device (DI 07290109014333), received between Apr 14, 2026 and May 26, 2026 — classified as 2 malfunctions.

The most frequently reported specific device problem is “Dull, Blunt” (1 report).

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 2 most recent of 2 reports, in the reporter's own words as published by the FDA.

• MalfunctionMay 26, 2026Mechanical Problem

  IT WAS REPORTED THAT THE TOOL RUSTED WITHIN 6 MONTHS OF PURCHASE.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 25285843 ↗
• MalfunctionApr 14, 2026Dull, Blunt

  IT WAS REPORTED THAT A PATIENT EXPERIENCED A TOOL MALFUNCTION; THE OSTEOTOMY TOOL IS BLUNT.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 24870590 ↗