FDA Adverse Event Injury Summary report: N

MINICAP TRANSFER SET

MDR report key: 3802610 · Received May 9, 2014

Report

Report Number
1416980-2014-14946
Event Type
Injury
Date Received
May 9, 2014
Date of Event
January 4, 2014
Report Date
April 14, 2014
Manufacturer
BAXTER HEALTHCARE - MOUNTAIN HOME
Product Code
KDJ
PMA / PMN Number
K882498
Adverse Event
Yes
Report Source
Manufacturer report
Reporter Location
NC, US
Reporter Occupation
NURSE

Narratives

Additional Manufacturer Narrative · 1

(B)(4). SHOULD ADDITIONAL RELEVANT INFORMATION BECOME AVAILABLE, A FOLLOW-UP REPORT WILL BE SUBMITTED. THIS IS THE SAME PATIENT AS (B)(4).

Additional Manufacturer Narrative · 1

(B)(4). A REVIEW OF ALL BATCH RECORD DOCUMENTS FOR POTENTIALLY ASSOCIATED LOT NUMBERS H13E08031, H13F05068, H13G26039, H13H08043, AND H13I06037 WAS PERFORMED WITH NO ISSUES NOTED DURING THE MANUFACTURING PROCESS. THERE WERE NO DEVIATIONS FROM STANDARD PROCEDURE AND NO EXCEPTIONS RELATED TO THE REPORTED CONDITION WERE NOTED. AS THE SAMPLE WAS NOT RETURNED A DEVICE ANALYSIS CANNOT BE COMPLETED. SHOULD ADDITIONAL RELEVANT INFORMATION BECOME AVAILABLE, A FOLLOW-UP WILL BE SUBMITTED.

Description of Event or Problem · 1

IT WAS REPORTED THAT A PATIENT EXPERIENCED PERITONITIS MANIFESTED BY ABDOMINAL PAIN COINCIDENT WITH PERITONEAL DIALYSIS (PD) THERAPY. THE CAUSE OF THE PERITONITIS WAS UNKNOWN. THE PATIENT WAS HOSPITALIZED FOR THE EVENT AND TREATED WITH UNSPECIFIED ANTIBIOTICS. THE PATIENT WAS DISCHARGED FROM THE HOSPITAL AFTER 12 DAYS AND WAS REPORTED TO BE RECOVERING FROM THE PERITONITIS. NO ADDITIONAL INFORMATION IS AVAILABLE. THIS IS REPORT 3 OF 3 INVOLVED IN THIS EVENT.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
281917 MINICAP TRANSFER SET SET, ADMINISTRATION, FOR PERITONEAL DIALYSIS, DISPOSABLE KDJ BAXTER HEALTHCARE - MOUNTAIN HOME

Patients

Seq Age Sex Outcome Treatment
1 44 YR Hospitalization| R EXTRANEAL VIAFLEX, MINICAP, CASSETTE| HOMECHOICE, 1.5% AND 2.5% DIANEAL PD4 AMBUFLEX| 1.5% AND 2.5% DIANEAL PD4 ULTRABAG