FDA Device Intelligence
HomeDevice types › KST

System, Blood Collection, Vacuum-Assisted, Manual

FDA product code KST · Class 1 · Hematology

80
Registered devices
71
Adverse events
4
Recalls
0
510(k) clearances

Devices with this code

Recent recalls

DateFirmReason
2015-10-01Hummingbird MedHummingbird Med Devices, Inc. is recalling ABG-HM-1 Hummi Micro Draw Blood Transfer because the connection between the "Hummi" Y connector and the yellow cannul
2015-03-11Hummingbird MedHummingbird Med Devices, Inc. is recalling the Hummi Micro Draw because of insertion difficulties.
2013-02-06Heritage Labs International LLCThe product has a Lithium Heparin contaminant which could adversely affect coagulation results potentially causing erroneous lab results.
2011-04-22Becton Dickinson & CompanyBD Vacutainer Push Button Blood Collection Set can potentially undergo cannula separation from the hub.

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