FDA Adverse Event Death Summary report: N

SET, ADMINISTRATION, FOR PERITONEAL DIALYSIS, DISPOSABLE

MDR report key: 4090255 · Received September 15, 2014

Report

Report Number
1416980-2014-31314
Event Type
Death
Date Received
September 15, 2014
Date of Event
August 20, 2014
Report Date
August 21, 2014
Manufacturer
BAXTER HEALTHCARE - SWINFORD
Product Code
KDJ
PMA / PMN Number
K894783
Adverse Event
Yes
Report Source
Manufacturer report
Reporter Location
IL, US
Reporter Occupation
NURSE

Narratives

Additional Manufacturer Narrative · 1

(B)(4). 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 SUPPLEMENTAL REPORT WILL BE SUBMITTED.

Additional Manufacturer Narrative · 1

(B)(4). THE REPORTED PRODUCT IS AN UNKNOWN BAXTER TITANIUM ADAPTER. SHOULD ADDITIONAL RELEVANT INFORMATION BECOME AVAILABLE, A SUPPLEMENTAL REPORT WILL BE SUBMITTED. THIS REPORT INVOLVES THE SAME PATIENT AS IN (B)(4).

Description of Event or Problem · 1

IT WAS REPORTED THAT A PATIENT PASSED AWAY COINCIDENT WITH AUTOMATED PERITONEAL DIALYSIS (APD) THERAPY. THE CAUSE OF DEATH WAS REPORTED TO BE DUE TO RENAL FAILURE, SEPSIS AND CARDIAC FAILURE. THE CAUSE OF THE SEPSIS EVENT WAS UNKNOWN. IT WAS REPORTED THAT THE PATIENT HAD BEEN HOSPITALIZED FOR AN UNKNOWN INDICATION AND SUBSEQUENTLY PASSED AWAY. TREATMENT WHILE HOSPITALIZED WAS UNKNOWN. IT WAS REPORTED THAT DURING HOSPITALIZATION PD THERAPY WAS DISCONTINUED AND THE PATIENT WAS PLACED ON HEMODIALYSIS. IT WAS UNKNOWN IF AN AUTOPSY WAS PERFORMED. ADDITIONAL INFORMATION WAS REQUESTED BUT IS NOT AVAILABLE. THIS IS REPORT 4 OF 4 INVOLVED IN THIS EVENT.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
568370 SET, ADMINISTRATION, FOR PERITONEAL DIALYSIS, DISPOSABLE KDJ BAXTER HEALTHCARE - SWINFORD

Patients

Seq Age Sex Outcome Treatment
1 47 YR Death| H DIANEAL PD4 2.5% AMBUFLEX, HOMECHOICE| DIANEAL PD4 4.25% AMBUFLEX,| TRANSFER SET, CASSETTE, MINICAP,