FDA Device Intelligence
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Set, Transfer (Blood/Plasma)

FDA product code KSB · Class 2 · Hematology

67
Registered devices
71
Adverse events
11
Recalls
6
510(k) clearances

Devices with this code

Recent recalls

DateFirmReason
2003-07-16Baxter Healthcare Corp.There are possible pinholes or perforations in the set tubing, caused by damage that occurred during the packaging process.
2003-07-16Baxter Healthcare Corp.There are possible pinholes or perforations in the set tubing, caused by damage that occurred during the packaging process.
2003-07-16Baxter Healthcare Corp.There are possible pinholes or perforations in the set tubing, caused by damage that occurred during the packaging process.
2003-07-16Baxter Healthcare Corp.There are possible pinholes or perforations in the set tubing, caused by damage that occurred during the packaging process.
2003-07-16Baxter Healthcare Corp.There are possible pinholes or perforations in the set tubing, caused by damage that occurred during the packaging process.
2002-12-18Baxter Healthcare Corp.Leakage may occur at the inlet port
2002-12-18Baxter Healthcare Corp.Leakage may occur at the inlet port
2002-12-18Baxter Healthcare Corp.Leakage may occur at the inlet port
2002-12-18Baxter Healthcare Corp.Leakage may occur at the inlet port
2002-12-18Baxter Healthcare Corp.Leakage may occur at the inlet port

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