FDA Adverse Event Death Summary report: N

SET, ADMINISTRATION, FOR PERITONEAL DIALYSIS, DISPOSABLE

MDR report key: 4223019 · Received November 4, 2014

Report

Report Number
1416980-2014-38654
Event Type
Death
Date Received
November 4, 2014
Report Date
October 8, 2014
Manufacturer
BAXTER HEALTHCARE - SWINFORD
Product Code
KDJ
PMA / PMN Number
K894783
Adverse Event
Yes
Report Source
Manufacturer report
Reporter Location
OH, US
Reporter Occupation
OTHER

Narratives

Additional Manufacturer Narrative · 1

(B)(4). THE REPORTED PRODUCT IS AN UNKNOWN BAXTER TITANIUM ADAPTER. THE DEVICE WAS NOT RETURNED AND THE LOT NUMBER OF THE DEVICE WAS UNKNOWN; THEREFORE, A SAMPLE ANALYSIS AND/OR A BATCH REVIEW COULD NOT BE COMPLETED. SHOULD ADDITIONAL RELEVANT INFORMATION BECOME AVAILABLE, A SUPPLEMENTAL REPORT WILL BE SUBMITTED. (B)(4).

Description of Event or Problem · 1

IT WAS REPORTED THAT A PATIENT EXPERIENCED PERITONITIS AND SUBSEQUENTLY PASSED AWAY COINCIDENT WITH PERITONEAL DIALYSIS (PD) THERAPY. THE CAUSE OF DEATH WAS SEPSIS AND PERITONITIS. THE CAUSE OF THE PERITONITIS WAS NOT REPORTED. IT WAS NOT REPORTED IF THE PATIENT WAS HOSPITALIZED FOR THE EVENTS PRIOR TO OR AT THE TIME OF DEATH. TREATMENT FOR THE SEPSIS AND PERITONITIS WAS NOT REPORTED. DIANEAL THERAPIES WERE REPORTED TO BE ONGOING PRIOR TO AND AT THE TIME OF DEATH, BUT IT WAS NOT REPORTED IF PERITONEAL DIALYSIS THERAPY WAS BEING PERFORMED WITH A BAXTER DEVICE AND/OR BAXTER SOLUTIONS PRIOR TO OR AT THE TIME OF DEATH. IT WAS NOT REPORTED IF THE PATIENT WAS RECOVERED FROM THE PERITONITIS EVENT PRIOR TO PASSING AWAY. IT WAS UNKNOWN IF AN AUTOPSY WAS PERFORMED. ADDITIONAL INFORMATION WAS REQUESTED, BUT IS NOT AVAILABLE. THIS IS REPORT 2 OF 3.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
707919 SET, ADMINISTRATION, FOR PERITONEAL DIALYSIS, DISPOSABLE KDJ BAXTER HEALTHCARE - SWINFORD

Patients

Seq Age Sex Outcome Treatment
1 Death DIANEAL 1.5% AND 2.5% AMBUFLEX,| TRANSFER SET, MINICAP