SET, ADMINISTRATION, FOR PERITONEAL DIALYSIS, DISPOSABLE
Report
- Report Number
- 1416980-2014-33519
- Event Type
- Injury
- Date Received
- September 26, 2014
- Report Date
- September 2, 2014
- Manufacturer
- BAXTER HEALTHCARE - MOUNTAIN HOME
- Product Code
- KDJ
- Adverse Event
- Yes
- Report Source
- Manufacturer report
- Reporter Location
- MO, US
- Reporter Occupation
- OTHER
Narratives
COMPLAINT NO: CMPLNT-(B)(4). THE REPORTED PRODUCT IS AN UNKNOWN BAXTER TRANSFER SET. AS THE SAMPLE WAS NOT RETURNED AND THE LOT NUMBER IS UNKNOWN, A DEVICE ANALYSIS CANNOT BE COMPLETED. SHOULD ADDITIONAL RELEVANT INFORMATION BECOME AVAILABLE, A FOLLOW UP REPORT WILL BE SUBMITTED. THIS IS SAME PATIENT AS IN CMPLNT-(B)(4), CMPLNT-(B)(4), AND CMPLNT-(B)(4).
IT WAS REPORTED THAT THE PATIENT EXPERIENCED PERITONITIS COINCIDENT WITH PERITONEAL DIALYSIS (PD) THERAPY. THE CAUSE OF THE PERITONITIS EVENT WAS UNKNOWN. THE PATIENT WAS NOT HOSPITALIZED FOR THE PERITONITIS. ON AN UNREPORTED DATE, THE PATIENT WAS TREATED WITH INJECTION GENTAMYCIN (INTRAPERITONEALLY, FOR 5 DAYS, DOSE AND FREQUENCY NOT REPORTED) AND CIPRO (ORALLY, DOSE, DURATION AND FREQUENCY NOT REPORTED) FOR PERITONITIS. THE PATIENT HAD RECOVERED FROM THE PERITONITIS EVENT AND SUBSEQUENTLY DIED DUE TO UNRELATED EVENTS. THE PD THERAPY WAS ONGOING DURING THE PERITONITIS EVENT. ADDITIONAL INFORMATION WAS REQUESTED BUT WAS NOT AVAILABLE AT THIS TIME. THIS IS REPORT 1 OF 4 INVOLVED IN THIS EVENT.
Devices
| Seq | Brand | Generic | Product Code | Manufacturer | Model | Lot | UDI-DI |
|---|---|---|---|---|---|---|---|
| 600412 | SET, ADMINISTRATION, FOR PERITONEAL DIALYSIS, DISPOSABLE | KDJ | BAXTER HEALTHCARE - MOUNTAIN HOME |
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 | Required Intervention | DIANEAL 1.5%, 2.5%, 4.25% ULTRABAG PD4,| DIANEAL 1.5% PD4 AMBUFLEX, HOMECHOICE| CASSETTE, TITANIUM ADAPTER, MINICAP |