Medical Action Industries 79069BRecalls & reported problems

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 10809160410400), received between Mar 17, 2026 and Mar 17, 2026 — classified as 1 malfunction.

The most frequently reported specific device problem is “Separation Problem” (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.

• MalfunctionMar 17, 2026Separation Problem

  THE CURVED HEMOSTAT FAILED TO HOLD DURING THE PROCEDURE, AS THE INSTRUMENT TIPS WOULD NOT REMAIN SECURED OR LOCKED IN PLACE. REPORTER INDICATED THERE WAS A DELAY OF A FEW MINUTES. RESIDENTS IN-TRAINING STATED THEY FEEL INTIMIDATED WHEN THE HEMOSTATS DO NOT HOLD UP DURING CIRCUMCISION PROCEDURE AND CAN CAUSE COSMETIC ISSUES.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 24617453 ↗