FDA Adverse Event Malfunction Summary report: N

FREEDOM CYCLER PD+

MDR report key: 506331 · Received December 24, 2003

Report

Report Number
2937457-2003-00032
Event Type
Malfunction
Date Received
December 24, 2003
Date of Event
December 4, 2003
Report Date
December 22, 2003
Manufacturer
FRESENIUS MEDICAL CARE-NORTH AMERICA
Product Code
KPF
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
CA, US
Reporter Occupation
OTHER

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1 FREEDOM CYCLER PD+ PERITONEAL DIALYSIS CYCLER KPF FRESENIUS MEDICAL CARE-NORTH AMERICA PD+ IQCARD NA

Patients

Seq Age Sex Outcome Treatment
1 NA