FDA Adverse Event Injury Summary report: N

SET, ADMINISTRATION, FOR PERITONEAL DIALYSIS, DISPOSABLE

MDR report key: 4103421 · Received September 19, 2014

Report

Report Number
1416980-2014-32464
Event Type
Injury
Date Received
September 19, 2014
Date of Event
August 21, 2014
Report Date
August 26, 2014
Manufacturer
BAXTER HEALTHCARE - SWINFORD
Product Code
KDJ
Adverse Event
Yes
Report Source
Manufacturer report
Reporter Location
KS
Reporter Occupation
OTHER

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 ADAPTOR. 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

THIS IS A REPORT OF A PATIENT WHO EXPERIENCED SEPSIS AND SUBSEQUENTLY PASSED AWAY COINCIDENT WITH PERITONEAL DIALYSIS (PD) THERAPY. THE CAUSE OF DEATH WAS REPORTED TO BE DUE TO SEPSIS. THE CAUSE OF THE SEPSIS WAS NOT REPORTED. IT WAS REPORTED THAT THE PATIENT WAS HOSPITALIZED FOR AN UNRELATED INDICATION. ON AN UNREPORTED DATE, THE PATIENT EXPERIENCED SEPSIS MANIFESTED BY FEVER, VOMITING AND DIARRHEA AND SUBSEQUENTLY PASSED AWAY. TREATMENT FOR THE EVENT OF SEPSIS WAS NOT REPORTED. PD THERAPY WAS REPORTED TO BE ONGOING. IT WAS UNKNOWN IF AN AUTOPSY WAS PERFORMED. NO ADDITIONAL INFORMATION IS AVAILABLE AT THIS TIME. THIS IS REPORT 3 OF 3 INVOLVED IN THIS EVENT.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
584026 SET, ADMINISTRATION, FOR PERITONEAL DIALYSIS, DISPOSABLE KDJ BAXTER HEALTHCARE - SWINFORD

Patients

Seq Age Sex Outcome Treatment
1 56 YR Death| H MINICAP, TITANIUM ADAPTER, 1.5% PHYSIONEAL,| 2.5% PHYSIONEAL, EXTRANEAL