FDA Adverse Event
Death
Summary report: N
LIBERTY CYCLER
MDR report key: 3873693
·
Received June 2, 2014
Report
- Report Number
- 2937457-2014-00907
- Event Type
- Death
- Date Received
- June 2, 2014
- Date of Event
- May 1, 2014
- Report Date
- May 2, 2014
- Manufacturer
- FRESENIUS MEDICAL CARE NORTH AMERICA
- Product Code
- FKX
- PMA / PMN Number
- K043363
- Adverse Event
- Yes
- Report Source
- Manufacturer report
- Reporter Location
- FL, US
- Reporter Occupation
- PATIENT FAMILY MEMBER OR FRIEND
Narratives
Additional Manufacturer Narrative · 1
A SUPPLEMENTAL REPORT WILL BE SUBMITTED UPON COMPLETION OF THE PT'S INVESTIGATION.
Description of Event or Problem · 1
A PERITONEAL DIALYSIS PT'S WIFE REPORTED THAT THE PT PASSED AWAY (EXACT DATE NOT PROVIDED). NO ADD'L INFO HAS BEEN PROVIDED ABOUT THE EVENT.
Devices
| Seq | Brand | Generic | Product Code | Manufacturer | Model | Lot | UDI-DI |
|---|---|---|---|---|---|---|---|
| 321772 | LIBERTY CYCLER | FKX | FRESENIUS MEDICAL CARE NORTH AMERICA |
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 | Death | PD SOLUTION| TUBING |