FDA Adverse Event Other Summary report: N

BAXTER HOMECHOICE

MDR report key: 306562 · Received November 20, 2000

Report

Report Number
306562
Event Type
Other
Date Received
November 20, 2000
Date of Event
June 19, 2000
Report Date
October 30, 2000
Manufacturer
BAXTER HEALTHCARE CORP, RENAL DIVISION
Product Code
KPF
Report Source
User Facility report
Reporter Location
IL, US
Reporter Occupation
NURSE

Narratives

Description of Event or Problem · 1

LEAK BETWEEN CASSETTE AND MEMBRANE GASKET.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1 BAXTER HOMECHOICE PD MACHINE KPF BAXTER HEALTHCARE CORP, RENAL DIVISION UNK UNK

Patients

Seq Age Sex Outcome Treatment
1 41 YR Other