MIS MD-IT100Recalls & reported problems

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 07290109007915), received between Jul 14, 2026 and Jul 14, 2026 — classified as 1 malfunction.

The most frequently reported specific device problem is “Physical Resistance/Sticking” (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 1 most recent of 1 reports, in the reporter's own words as published by the FDA.

• MalfunctionJul 14, 2026Physical Resistance/Sticking

  IT WAS REPORTED THAT THERE WAS A MALFUNCTION WHERE THE CAP DOES NOT COME OFF THE TRANSFER BODY.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 25815874 ↗