EZout 7812044001KRecalls & reported problems

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 07613327294453), received between May 2, 2017 and May 2, 2017 — classified as 1 malfunction.

The most frequently reported specific device problem is “Break” (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. What reports can and can't tell you · How this data works · Data updated Oct 18, 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.

• MalfunctionMay 2, 2017Break; Break

  IT WAS REPORTED THAT DURING A REPLACEMENT SURGERY PROCEDURE, AFTER REMOVING THE SOCKET, THE EZOUT SAW BLADE BROKE, THE BROKEN BLADE WAS REMOVED USING FORCEPS. IT WAS ALSO REPORTED THAT THERE WAS NO DELAY AND NO ADVERSE CONSEQUENCES AS A RESULT OF THIS EVENT. IT WAS FURTHER REPORTED THAT THE PROCEDURE WAS COMPLETED SUCCESSFULLY.

  Patient problems: No Consequences Or Impact To Patient

  MAUDE report 6536789 ↗