MIS CS-MAN10Recalls & reported problems

Summary

The FDA's MAUDE database contains 2 adverse event reports that list this exact device (DI 07290109010557), received between Jun 3, 2026 and Jun 3, 2026 — classified as 2 malfunctions.

The most frequently reported specific device problem is “Mechanical Problem” (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 2 most recent of 2 reports, in the reporter's own words as published by the FDA.

• MalfunctionJun 3, 2026Mechanical Problem

  IT WAS REPORTED THAT THERE WAS A TOOL MALFUNCTION WHERE THE INTERNAL HEX OF THE DIGITAL ANALOG IS DEFECTIVE, AS THE SCREW COULD NOT BE THREADED IN.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 25374463 ↗
• MalfunctionJun 3, 2026Mechanical Problem

  IT WAS REPORTED THAT THERE WAS A TOOL MALFUNCTION WHERE AN INTERNAL HEX OF THE DIGITAL ANALOG IS DEFECTIVE, AS THE SCREW COULD NOT BE THREADED IN.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 25374424 ↗