Integra® Ruggles®-Redmond™ NHI10Recalls & reported problems

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 10381780149187), received between Aug 5, 2022 and Aug 5, 2022 — classified as 1 malfunction.

The most frequently reported specific device problem is “Electrical /Electronic Property 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.

• MalfunctionAug 5, 2022Electrical /Electronic Property Problem; Electrical /Electronic Property Problem

  THIS IS 2 OF 2 REPORTS FOR THE BIPOLAR FORCEPS REPORTEDLY USED DURING THIS EVENT AND IS LINKED TO MFG REPORT NUMBER 3014334038-2022-00170. A FACILITY REPORTED THAT DURING AN ORTHO/SPINE PROCEDURE, IT WAS NOTED THAT THE BIPOLAR FORCEPS/BUZZ NONSTICK (NHI15) WERE NO LONGER CONDUCTING AT THE TIPS. IT WAS REPORTED THAT THERE WAS A DELAY OF 30 MINUTES TO AN HOUR BECAUSE THE STAFF HAD TO OPEN REPLACEMENT INSTRUMENTS. THE PROCEDURE WAS COMPLETED WITH REPLACEMENT INSTRUMENTS. NO PATIENT INJURY OCCURRED.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 15175104 ↗