FDA Adverse Event Injury Summary report: N

SET, ADMINISTRATION, FOR PERITONEAL DIALYSIS, DISPOSABLE

MDR report key: 4123590 · Received September 26, 2014

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

Additional Manufacturer Narrative · 1

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).

Description of Event or Problem · 1

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