FDA Adverse Event Injury Summary report: N

SET, ADMINISTRATION, FOR PERITONEAL DIALYSIS, DISPOSABLE

MDR report key: 2192417 · Received August 5, 2011

Report

Report Number
1423500-2011-10294
Event Type
Injury
Date Received
August 5, 2011
Date of Event
July 1, 2011
Report Date
July 18, 2011
Manufacturer
BAXTER HEALTHCARE
Product Code
KDJ
Adverse Event
Yes
Report Source
Manufacturer report
Reporter Location
AS
Reporter Occupation
OTHER

Narratives

Additional Manufacturer Narrative · 1

(B)(4). THE DEVICES INVOLVED IN THE INCIDENT WERE UNKNOWN. AS THE DATE OF ONSET OF THIS PERITONITIS EPISODE IS UNKNOWN AND PATIENTS DISCARD SUPPLIES AFTER EACH THERAPY, THE SAMPLE WAS NOT REQUESTED. A 510K NUMBER WILL NOT BE PROVIDED IN THE MDR AS THE PRODUCT CODE AND LOT NUMBER ARE UNKNOWN. SINCE THE LOT NUMBER IS UNKNOWN, NO BATCH REVIEW WILL BE PERFORMED. BAXTER HAS RECEIVED SIMILAR REPORTS FOR THE REPORTED PROBLEM. THE ROOT CAUSE INVESTIGATION IS IN PROGRESS. THE ROOT CAUSE OF THE REPORTED CONDITION OF PERITONITIS IS UNDETERMINED.

Description of Event or Problem · 1

THIS REPORT WAS RECEIVED FROM (B)(4) AND IS A SPONTANEOUS REPORT BY A CONSUMER FROM (B)(6) OF PERITONITIS IN A PATIENT COINCIDENT WITH EXTRANEAL VIAFLEX, DIANEAL PD4 FREELINE SOLO 1.5% AND DIANEAL PD4 FREELINE SOLO 2.5% THERAPIES FOR PERITONEAL DIALYSIS (PD). ON (B)(6) 2011, THE PATIENT EXPERIENCED PERITONITIS. THE CAUSE OF THE PERITONITIS WAS UNKNOWN. ON AN UNREPORTED DATE, THE PATIENT BEGAN AN UNKNOWN ANTIBIOTIC. THE EVENT OF PERITONITIS WAS RESOLVING. EXTRANEAL VIAFLEX, DIANEAL PD4 FREELINE SOLO 1.5% AND DIANEAL PD4 FREELINE SOLO 2.5% AS WELL AS UNKNOWN ANTIBIOTIC THERAPY WERE ONGOING. THE REPORTER DID NOT PROVIDE AN OPINION OF CAUSALITY.

Devices

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

Patients

Seq Age Sex Outcome Treatment
1 80 YR Required Intervention EXTRANEAL VIAFLEX| DIANEAL PD4 FREELINE SOLO 2.5%| DIANEAL PD4 FREELINE SOLO 1.5%