FDA Device Intelligence
HomeDevice types › BZD

Ventilator, Non-Continuous (Respirator)

FDA product code BZD · Class 2 · Anesthesiology

5,435
Registered devices
300,868
Adverse events
81
Recalls
461
510(k) clearances

Devices with this code

Recent 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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Sourced from public U.S. FDA data. Informational only — not medical or regulatory advice. Not affiliated with the FDA.