HUDSON RCI IPN046955Recalls & reported problems

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 14026704343963), received between May 7, 2021 and May 7, 2021 — 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 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 7, 2021Material Separation; Material Separation

  MAUDE REPORT: IT WAS REPORTED "THE PATIENT WAS ON A HIGH FLOW NANSAL CANNULA AND UPON ASSESSMENT, THE RN NOTED THAT THE TUBING THAT DIRECTLY CONNECTS THE PIECE UNDER THE PATIENT'S NOSE BROKE OFF FROM THE NOSE ATTACHMENT". NO PATIENT HARM OR INJURY REPORTED. PATIENT CONDITION NOT REPORTED.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 11794178 ↗