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Bassinet, Hospital

FDA product code NZG · Class 2 · General Hospital

87
Registered devices
104
Adverse events
2
Recalls
0
510(k) clearances

Devices with this code

Recent recalls

DateFirmReason
2018-10-10Stryker Medical Division of Stryker CorporationIt was identified that the volume of air inside the mattress may expand in regions of high altitude which may result in an unintended gap between the plateau of
2011-10-14Nemschoff Chairs, Inc.To correct issues with casters, door hinges, drawer slides, and the bassinet surround. Also, to add labeling to the product regarding specific instructions for

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