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Injector, Fluid, Non-Electrically Powered

FDA product code KZE · Class 2 · General Hospital

16
Registered devices
467
Adverse events
1
Recalls
53
510(k) clearances

Devices with this code

Recent recalls

DateFirmReason
2010-06-01CaridianBCT, Inc.Labeling clarification and software updates to include fixes for end of run summaries, increasing boot reliability, corrections to the double red blood cell cou

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Linked GUDID · 510(k)/PMA · MAUDE · recalls · establishments. Free tier, no card required.

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