NA 702927Recalls & reported problems

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 04546540402042), received between Sep 25, 2015 and Sep 25, 2015 — 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 16, 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.

• MalfunctionSep 25, 2015Break

  DURING SURGERY IT WAS REPORTED THAT SURGEON TURNED FORCEPS TIGHTLY TO REPOSITION AND THE FORCEPS SNAPPED. NO DELAY OR ADVERSE CONSEQUENCE TO PATIENT OR USER.

  Patient problems: No Consequences Or Impact To Patient

  MAUDE report 5104245 ↗