FDA Device Intelligence
HomeDevice types › NVP

Holding Chambers, Direct Patient Interface

FDA product code NVP · Class 2 · Anesthesiology

101
Registered devices
14
Adverse events
3
Recalls
16
510(k) clearances

Devices with this code

Recent recalls

DateFirmReason
2021-03-16Cardinal Health Inc.Due to shipping delays the devices were exposed to temperature excursions of 31.9F, intermittently over a 2 hour and 15 minute period of time which may cause in
2021-03-16Cardinal Health Inc.Due to shipping delays the devices were exposed to temperature excursions of 31.9F, intermittently over a 2 hour and 15 minute period of time which may cause in
2016-05-16FSC Laboratories, IncProduct had torn/loose seal around the mouthpiece.

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