Home › FISHER & PAYKEL HEALTHCARE LIMITED › Fisher & Paykel Healthcare
Fisher & Paykel Healthcare
FISHER & PAYKEL HEALTHCARE LIMITED · Model 400481 · UDI-DI 09420012426765
BZD
Prescription
10
510(k) clearances
303,210
Adverse events (4,572 deaths)
83
Recalls
119
Facilities
Description
F&P Simplus Full Face Mask - Large/Large
Recalls
| Date | Firm | Reason |
|---|---|---|
| 2026-08-11 | CooperSurgical, Inc. | Potential to exhibit a loose connection between the flexible tubing and the nasal cannula, during assembly or while in use, which may result in loss of CPAP pressure, possibly redu |
| 2026-08-11 | CooperSurgical, Inc. | Potential to exhibit a loose connection between the flexible tubing and the nasal cannula, during assembly or while in use, which may result in loss of CPAP pressure, possibly redu |
| 2025-06-30 | Philips Respironics, Inc. | Devices may possess a programming error resulting in an incorrect device configuration. |
| 2025-06-30 | Philips Respironics, Inc. | Devices may possess a programming error resulting in an incorrect device configuration. |
| 2025-06-30 | Philips Respironics, Inc. | Devices may possess a programming error resulting in an incorrect device configuration. |
| 2024-03-01 | SleepNet Corporation | Update to contraindications and warning language due to CPAP masks containing magnets. |
| 2024-03-01 | SleepNet Corporation | Update to contraindications and warning language due to CPAP masks containing magnets. |
| 2024-03-01 | SleepNet Corporation | Update to contraindications and warning language due to CPAP masks containing magnets. |
| 2024-03-01 | SleepNet Corporation | Update to contraindications and warning language due to CPAP masks containing magnets. |
| 2024-03-01 | SleepNet Corporation | Update to contraindications and warning language due to CPAP masks containing magnets. |
Query this across every FDA database — by API.
Linked GUDID · 510(k)/PMA · MAUDE · recalls · establishments. Free tier, no card required.
Get your free API keyRead the docsData 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.
