FISHER & PAYKEL HEALTHCARE 900MR190Recalls & reported problems

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 09420012429780), received between Feb 23, 2023 and Feb 23, 2023 — classified as 1 malfunction.

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

• MalfunctionFeb 23, 2023Break; Break

  A HEALTHCARE FACILITY IN CANADA REPORTED VIA A FISHER & PAYKEL HEALTHCARE (F&P) FIELD REPRESENTATIVE, THAT THE CLAMP OF A 900MR190 WATER FEEDSET WAS FOUND BROKEN DURING USE CAUSING THE MR250 MANUAL FEED ADULT HUMIDIFICATION CHAMBER TO OVERFILL. IT WAS ALSO REPORTED THAT THE "WATER FLOWED INTO THE PATIENT'S BREATHING CIRCUIT AND INTO THE PATIENT'S AIRWAY". THERE WERE NO ADVERSE PATIENT OUTCOMES REPORTED AS A RESULT OF THIS EVENT. HOWEVER, FURTHER INFORMATION HAS BEEN REQUESTED.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 16433244 ↗