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 |