SET, ADMINISTRATION, FOR PERITONEAL DIALYSIS, DISPOSABLE
Report
- Report Number
- 1423500-2011-10299
- Event Type
- Injury
- Date Received
- August 5, 2011
- Date of Event
- January 1, 2011
- Report Date
- July 18, 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 (B)(4) AND IS A SPONTANEOUS REPORT BY A NURSE FROM (B)(6) OF (B)(6) IN A PATIENT COINCIDENT WITH DIANEAL PD4 ULTRABAG THERAPY FOR CONTINUOUS AMBULATORY PERITONEAL DIALYSIS (CAPD). ON AN UNREPORTED DATE IN 2011, THE PATIENT EXPERIENCED BACTERIAL PERITONITIS FROM AN UNKNOWN CAUSE. IT WAS NOT REPORTED WHETHER THE PATIENT WAS HOSPITALIZED, IF REMEDIAL THERAPY WAS RENDERED, OR IF THE EVENT OF (B)(6) RESOLVED. IT WAS NOT REPORTED WHETHER DIANEAL PD4 ULTRABAG THERAPY WAS ONGOING. THE NURSE STATED THAT THE EVENT OF (B)(6) WAS NOT RELATED TO DIANEAL PD4 ULTRABAG THERAPY.
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 | 69 YR | Other | DIANEAL PD4 ULTRABAG |