Fisher & Paykel Healthcare 900MR810Recalls & reported problems
Fisher & Paykel Healthcare Limited · Adult single limb circuit inspiratory heated for use with MR810 only · Class 2
Data updated Oct 18, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 14
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 14 adverse event reports that list this exact device (DI 09420012432247), received between Aug 17, 2020 and Jan 19, 2025 — classified as 14 malfunctions.
The most frequently reported specific device problem is “Break” (13 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
- Break13
- Device Handling Problem1
- Material Puncture/Hole1
- Melted1
Patient problems
- No Clinical Signs, Symptoms or Conditions14
- No Patient Involvement1
Recent adverse event reports
The 14 most recent of 14 reports, in the reporter's own words as published by the FDA.
MalfunctionJan 19, 2025Melted; Melted
A DISTRIBUTOR IN CALIFORNIA REPORTED VIA A FISHER & PAYKEL HEALTHCARE (F&P) FIELD REPRESENTATIVE THAT THE 900MR810 ADULT HEATED WALL REUSABLE BREATHING CIRCUIT HAD MELTED. THERE WAS NO PATIENT INVOLVEMENT AS THE ISSUE WAS FOUND WHILST THE DEVICE WAS NOT IN USE ON A PATIENT.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 21188189 ↗MalfunctionDec 21, 2023Break; Break
A HEALTHCARE FACILITY IN TAIWAN REPORTED, VIA A FISHER & PAYKEL HEALTHCARE (F&P) FIELD REPRESENTATIVE, THAT A 900MR810 ADULT HEATED WALL REUSABLE BREATHING CIRCUIT WAS DAMAGED. THERE WAS NO REPORTED PATIENT CONSEQUENCE.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 18371585 ↗MalfunctionDec 21, 2023Break; Material Puncture/Hole; Break; Material Puncture/Hole
A HEALTHCARE FACILITY IN TAIWAN REPORTED, VIA A FISHER & PAYKEL HEALTHCARE (F&P) FIELD REPRESENTATIVE, THAT A 900MR810 ADULT HEATED WALL REUSABLE BREATHING CIRCUIT WAS DAMAGED. THERE WAS NO REPORTED PATIENT CONSEQUENCE.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 18371584 ↗MalfunctionDec 6, 2023Break; Break
A HEALTHCARE FACILITY IN TAIWAN REPORTED, VIA A FISHER & PAYKEL HEALTHCARE (F&P) FIELD REPRESENTATIVE, THAT A 900MR810 ADULT HEATED WALL REUSABLE BREATHING CIRCUIT WAS DAMAGED. THERE WAS NO REPORTED PATIENT CONSEQUENCE.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 18279919 ↗MalfunctionApr 30, 2023Break; Break
A HEALTHCARE FACILITY IN TAIWAN REPORTED VIA A FISHER AND PAYKEL (F&P) HEALTHCARE REPRESENTATIVE THAT THE TUBING OF 900MR810 1.5M ADULT HEATED WALL REUSABLE CIRCUIT WAS DAMAGED. THERE WAS NO PATIENT INVOLVEMENT.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 16841423 ↗MalfunctionDec 13, 2022Break; Break
A HEALTHCARE FACILITY IN TAIWAN REPORTED, VIA A FISHER & PAYKEL HEALTHCARE (F&P) FIELD REPRESENTATIVE, THAT FIFTEEN 900MR810 ADULT HEATED WALL REUSABLE BREATHING CIRCUIT'S WERE DAMAGED. THERE WAS NO PATIENT INVOLVEMENT AS THE ISSUE WAS FOUND WHILST THE CIRCUIT WAS NOT IN USE ON A PATIENT.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 15965601 ↗MalfunctionNov 23, 2022Break; Break
A HEALTHCARE FACILITY IN TAIWAN REPORTED VIA A FISHER AND PAYKEL (F&P) HEALTHCARE REPRESENTATIVE THAT THE TUBING OF 900MR810 1.5M ADULT HEATED WALL REUSABLE CIRCUIT WAS DAMAGED. THERE WAS NO REPORTED PATIENT CONSEQUENCE.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 15856653 ↗MalfunctionAug 18, 2022Break
A DISTRIBUTOR IN NEW YORK, REPORTED THAT A 900MR810 ADULT HEATED WALL REUSABLE BREATHING CIRCUIT WAS DAMAGED DURING USE. THERE WAS NO REPORTED PATIENT CONSEQUENCE.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 15255964 ↗MalfunctionMay 18, 2022Break; Break
A HEALTHCARE FACILITY IN (B)(6), REPORTED THAT A 900MR810 ADULT HEATED WALL REUSABLE BREATHING CIRCUIT WAS DAMAGED DURING USE. THERE WAS NO REPORTED PATIENT CONSEQUENCE.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 14431879 ↗MalfunctionApr 22, 2022Break
A HEALTHCARE FACILITY IN (B)(6) REPORTED VIA A FISHER & PAYKEL HEALTHCARE (F&P) FIELD REPRESENTATIVE THAT FIVE 900MR810 ADULT HEATED WALL REUSABLE BREATHING CIRCUITS WERE DAMAGED DURING USE. THERE WAS NO PATIENT CONSEQUENCE.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 14183959 ↗MalfunctionMar 8, 2022Break; Break
A CONSUMER IN (B)(6) REPORTED THAT A 900MR810 ADULT HEATED WALL REUSABLE BREATHING CIRCUIT WAS DAMAGED DURING USE. THERE WAS NO PATIENT CONSEQUENCE.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 13697975 ↗MalfunctionDec 22, 2021Break
A CONSUMER IN (B)(6) REPORTED THAT TWO 900MR810 ADULT HEATED WALL REUSABLE BREATHING CIRCUITS WERE DAMAGED DURING USE. THERE WAS NO REPORTED PATIENT CONSEQUENCE.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 13058414 ↗MalfunctionJun 9, 2021Break; Break
A HEALTHCARE FACILITY IN (B)(6) REPORTED, VIA A FISHER & PAYKEL HEALTHCARE (F&P) FIELD REPRESENTATIVE, THAT A 900MR810 ADULT HEATED WALL REUSABLE BREATHING CIRCUIT WAS DAMAGED. THERE WAS NO REPORTED PATIENT CONSEQUENCE.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 11972058 ↗MalfunctionAug 17, 2020Break; Device Handling Problem; Device Handling Problem
A HEALTHCARE FACILITY IN (B)(6) REPORTED THAT A 900MR810 ADULT HEATED WALL REUSABLE BREATHING CIRCUIT WAS DAMAGED. THERE WAS NO PATIENT INVOLVEMENT.
Patient problems: No Clinical Signs, Symptoms or Conditions; No Patient Involvement
MAUDE report 10417819 ↗
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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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