FDA Device Intelligence
HomeDevice types › KPF

System, Dialysate Delivery, Semi-Automatic, Peritoneal

FDA product code KPF · Class 2 · Gastroenterology, Urology

0
Registered devices
161
Adverse events
5
Recalls
13
510(k) clearances

Recent recalls

DateFirmReason
2007-11-14Baxter Healthcare Renal DivPre-Treatment/Post-Treatment Report errors: 1) The Heparin Bolus Value is displayed on Pre and Post Treatment Reports for patients with "No Heparin" orders (Ren
2007-11-14Baxter Healthcare Renal DivPre-Treatment/Post-Treatment Report errors: 1) The Heparin Bolus Value is displayed on Pre and Post Treatment Reports for patients with "No Heparin" orders (Ren
2006-03-29Baxter Healthcare Renal DivSoftware Error: There are software discrepancies that may increase the possibility of a medication error if the dialysis clinic software is used to track, recor
2006-03-29Baxter Healthcare Renal DivSoftware Error: There are software discrepancies that may increase the possibility of a medication error if the dialysis clinic software is used to track, recor
2006-03-29Baxter Healthcare Renal DivSoftware Error: There are software discrepancies that may increase the possibility of a medication error if the dialysis clinic software is used to track, recor

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