n.a. 840036ERecalls & reported problems

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 04048551207826), received between Jul 29, 2019 and Jul 29, 2019 — classified as 1 malfunction.

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

• MalfunctionJul 29, 2019Material Separation; Material Separation

  ALLEGEDLY, DURING A LARYNGOSCOPY WHEN PULLING OUT THE ELECTRODE THE DOCTOR NOTICED THE TIP WAS MISSING. PER THE NURSE MANAGER, "THE DOCTOR WAS ABLE TO REMOVE THE TIP IN IT'S ENTIRETY, THE CASE COMPLETED WITH NO HARM TO PATIENT".

  Patient problems: No Consequences Or Impact To Patient

  MAUDE report 8836800 ↗