FDA Device Intelligence
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Fisher & Paykel Healthcare

FISHER & PAYKEL HEALTHCARE LIMITED · Model 400421SL · UDI-DI 09420012427090

BZD Prescription
1
510(k) clearances
303,210
Adverse events (4,572 deaths)
81
Recalls
118
Facilities

Description

F&P Pilairo Q Nasal Pillows Mask - SL

Recalls

DateFirmReason
2025-06-30Philips Respironics, Inc.Devices may possess a programming error resulting in an incorrect device configuration.
2025-06-30Philips Respironics, Inc.Devices may possess a programming error resulting in an incorrect device configuration.
2025-06-30Philips Respironics, Inc.Devices may possess a programming error resulting in an incorrect device configuration.
2024-03-01SleepNet CorporationUpdate to contraindications and warning language due to CPAP masks containing magnets.
2024-03-01SleepNet CorporationUpdate to contraindications and warning language due to CPAP masks containing magnets.
2024-03-01SleepNet CorporationUpdate to contraindications and warning language due to CPAP masks containing magnets.
2024-03-01SleepNet CorporationUpdate to contraindications and warning language due to CPAP masks containing magnets.
2024-03-01SleepNet CorporationUpdate to contraindications and warning language due to CPAP masks containing magnets.
2024-03-01SleepNet CorporationUpdate to contraindications and warning language due to CPAP masks containing magnets.
2024-03-01SleepNet CorporationUpdate to contraindications and warning language due to CPAP masks containing magnets.

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Data compiled from public U.S. FDA sources (GUDID, 510(k)/PMA, MAUDE, recalls, establishment registration). Adverse-event reports are unverified and do not establish causation. Informational only — not medical, clinical, or regulatory advice.