Fisher & Paykel Healthcare RT210Recalls & reported problems
Fisher & Paykel Healthcare Limited · Adult ventilator circuit dual heated with MR290 autofeed chamber · Class 2
Data updated Oct 18, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 2
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 2 adverse event reports that list this exact device (DI 09420012430298), received between Mar 25, 2025 and Mar 25, 2025 — classified as 2 malfunctions.
The most frequently reported specific device problem is “Gas/Air Leak” (2 reports).
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.
Reports received per month
Most reported problems
Device problems
- Gas/Air Leak2
Patient problems
- No Clinical Signs, Symptoms or Conditions2
Recent adverse event reports
The 2 most recent of 2 reports, in the reporter's own words as published by the FDA.
MalfunctionMar 25, 2025Gas/Air Leak; Gas/Air Leak
A HEALTHCARE FACILITY IN NEW JERSEY REPORTED THAT TWO MR290V VENTED AUTOFEED HUMIDIFICATION CHAMBERS PROVIDED WITH THE RT210 ADULT VENTILATOR CIRCUIT WERE FOUND LEAKING AIR DURING PATIENT USE. THERE WAS NO REPORTED PATIENT HARM.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 21694497 ↗MalfunctionMar 25, 2025Gas/Air Leak; Gas/Air Leak
A HEALTHCARE FACILITY IN NEW JERSEY REPORTED THAT FOUR RT210 ADULT VENTILATOR CIRCUITS FAILED THE VENTILATOR LEAK TEST PRIOR TO PATIENT USE. THE ISSUE REPORTEDLY RESOLVED WHEN THE MR290V VENTED AUTOFEED HUMIDIFICATION CHAMBERS PROVIDED WITH THE RT210 ADULT VENTILATOR CIRCUITS WERE REPLACED. THERE WAS NO REPORTED PATIENT INVOLVEMENT.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 21694496 ↗
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Sources and updates
- Device record: FDA GUDID, file dated Oct 13, 2026 · View this device in AccessGUDID ↗
- Adverse event reports: FDA MAUDE, file dated Oct 14, 2026 · each report above links to its original FDA record
- Recalls: FDA Medical Device Recalls, file dated Oct 16, 2026
- Page last rebuilt: Oct 18, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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