FDA Adverse Event Injury Summary report: N

SET, ADMINISTRATION, FOR PERITONEAL DIALYSIS, DISPOSABLE

MDR report key: 4203055 · Received October 27, 2014

Report

Report Number
1416980-2014-37554
Event Type
Injury
Date Received
October 27, 2014
Date of Event
September 25, 2014
Report Date
September 29, 2014
Manufacturer
BAXTER HEALTHCARE - MOUNTAIN HOME
Product Code
KDJ
Adverse Event
Yes
Report Source
Manufacturer report
Reporter Location
NY, US
Reporter Occupation
OTHER

Narratives

Additional Manufacturer Narrative · 1

(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 EVALUATION CANNOT BE COMPLETED. SHOULD ADDITIONAL RELEVANT INFORMATION BECOME AVAILABLE, A SUPPLEMENTAL REPORT WILL BE SUBMITTED. SAME PATIENT AS (B)(4).

Description of Event or Problem · 1

IT WAS REPORTED THAT A PERITONEAL DIALYSIS (PD) PATIENT EXPERIENCED BACTERIAL INFECTION. THE BACTERIAL INFECTION WAS MANIFESTED BY CLOUDY EFFLUENT ALONG WITH SYMPTOMS OF CHILLS, ABDOMINAL PAIN AND FEVER. THE SAME DAY, THE PATIENT WAS HOSPITALIZED FOR THE EVENT. THE CAUSE OF THE BACTERIAL INFECTION WAS NOT REPORTED. TREATMENT AND OUTCOME WERE NOT REPORTED. FOUR DAYS AFTER ADMISSION TO THE HOSPITAL, THE PATIENT WAS DISCHARGED. PD THERAPY WAS ONGOING. ADDITIONAL INFORMATION WAS NOT AVAILABLE. THIS IS REPORT 1 OF 3 INVOLVED IN THIS PERITONITIS EVENT.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
681866 SET, ADMINISTRATION, FOR PERITONEAL DIALYSIS, DISPOSABLE KDJ BAXTER HEALTHCARE - MOUNTAIN HOME

Patients

Seq Age Sex Outcome Treatment
1 37 YR Hospitalization DIANEAL PD4 1.5 AND 2.5% AMBUFLEX AND ULTRABAG| TITANIUM ADAPTER, MINI-CAP, EXTRANEAL