Skip to content

Fisher & Paykel Healthcare RT324Recalls & reported problems

Fisher & Paykel Healthcare Limited · Infant continuous flow circuit (> 4 L/min) single heated with MR290 autofeed chamber · Class 2

Data updated Oct 18, 2026 from official FDA records · Editorial policy

Adverse event reports
1
Deaths reported
0
Injuries reported
0
Recalls naming it
0

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 09420012431127), received between Feb 2, 2021 and Feb 2, 2021 — classified as 1 malfunction.

The most frequently reported specific device problem is “Connection 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

Device problems

  • Connection Problem1
  • Disconnection1

Patient problems

  • No Clinical Signs, Symptoms or Conditions1

Recent adverse event reports

The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.

  • MalfunctionFeb 2, 2021Disconnection; Disconnection; Connection Problem

    A HEALTHCARE FACILITY IN IRELAND REPORTED VIA A FISHER & PAYKEL HEALTHCARE (F&P) FIELD REPRESENTATIVE THAT THE PRESSURE LINE COMPONENT OF THREE RT324 INFANT CONTINUOUS FLOW BREATHING CIRCUITS WAS NOT CONNECTING PROPERLY TO A VIASYS VENTILATOR. THERE WAS NO REPORTED PATIENT CONSEQUENCE.

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 11270471 ↗

Other Humidifier, Respiratory Gas, (Direct Patient Interface) devices

All Humidifier, Respiratory Gas, (Direct Patient Interface) devices →

Sources and updates

How reports and recalls are matched · Editorial policy · Report an error on this page