SET, ADMINISTRATION, FOR PERITONEAL DIALYSIS, DISPOSABLE
Report
- Report Number
- 1423500-2011-10756
- Event Type
- Injury
- Date Received
- August 16, 2011
- Date of Event
- January 1, 2011
- Report Date
- July 28, 2011
- Manufacturer
- BAXTER HEALTHCARE
- Product Code
- KDJ
- Adverse Event
- Yes
- Report Source
- Manufacturer report
- Reporter Location
- TW
- Reporter Occupation
- NURSE
Narratives
(B)(4). THE DEVICES INVOLVED IN THE INCIDENT WERE UNKNOWN. AS THE DATE OF ONSET OF THIS PERITONITIS EPISODE IS UNKNOWN AND PATIENTS DISCARD SUPPLIES AFTER EACH THERAPY, THE SAMPLE WAS NOT REQUESTED. A 510K NUMBER WILL NOT BE PROVIDED IN THE MDR AS THE PRODUCT CODE AND LOT NUMBER ARE UNKNOWN. SINCE THE LOT NUMBER IS UNKNOWN, NO BATCH REVIEW WILL BE PERFORMED. BAXTER HAS RECEIVED SIMILAR REPORTS FOR THE REPORTED PROBLEM. THE ROOT CAUSE INVESTIGATION IS IN PROGRESS. THE ROOT CAUSE OF THE REPORTED CONDITION OF PERITONITIS IS UNDETERMINED.
THIS REPORT WAS RECEIVED FROM GLOBAL PHARMACOVIGILANCE (GPV) AND IS A SPONTANEOUS REPORT BY A NURSE FROM (B)(6) OF PERITONITIS IN A PATIENT COINCIDENT WITH DIANEAL PD2 AMBUFLEX AND EXTRANEAL VIAFLEX THERAPIES FOR AUTOMATED PERITONEAL DIALYSIS (APD). IN 2011, THE PATIENT EXPERIENCED PERITONITIS DUE TO AN UNKNOWN CAUSE. IT WAS NOT REPORTED WHETHER THE PATIENT WAS HOSPITALIZED OR IF REMEDIAL THERAPY WAS RENDERED. IT WAS NOT REPORTED WHETHER THE EVENT OF PERITONITIS RESOLVED OR WHETHER DIANEAL PD2 AMBUFLEX OR EXTRANEAL VIAFLEX THERAPIES WERE ONGOING. THE NURSE DID NOT PROVIDE A STATEMENT OF CAUSALITY FOR THE EVENT OF PERITONITIS.
Devices
| Seq | Brand | Generic | Product Code | Manufacturer | Model | Lot | UDI-DI |
|---|---|---|---|---|---|---|---|
| 1 | SET, ADMINISTRATION, FOR PERITONEAL DIALYSIS, DISPOSABLE | KDJ | BAXTER HEALTHCARE |
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 | Other | EXTRANEAL VIAFLEX| DIANEAL PD2 AMBUFLEX| PD CYCLER |