FDA Adverse Event Injury Summary report: N

MINICAP TRANSFER SET

MDR report key: 3803063 · Received May 9, 2014

Report

Report Number
1416980-2014-15032
Event Type
Injury
Date Received
May 9, 2014
Date of Event
April 12, 2014
Report Date
April 15, 2014
Manufacturer
BAXTER HEALTHCARE - MOUNTAIN HOME
Product Code
KDJ
PMA / PMN Number
K882498
Adverse Event
Yes
Report Source
Manufacturer report
Reporter Location
GA, US
Reporter Occupation
NURSE

Narratives

Additional Manufacturer Narrative · 1

(B)(4). A REVIEW OF ALL BATCH RECORD DOCUMENTS WAS PERFORMED FOR POTENTIALLY ASSOCIATED LOT NUMBERS H13I04032, H13I10047, AND H13I27025 WITH NO ISSUES NOTED DURING THE MANUFACTURING PROCESS. THERE WERE NO DEVIATIONS FROM STANDARD PROCEDURE AND NO EXCEPTIONS RELATED TO THE REPORTED CONDITION. SHOULD ADDITIONAL RELEVANT INFORMATION BECOME AVAILABLE, A FOLLOW-UP WILL BE SUBMITTED. THIS IS THE SAME PATIENT AS (B)(4).

Description of Event or Problem · 1

IT WAS REPORTED THAT A PERITONEAL DIALYSIS (PD) PATIENT (PT) EXPERIENCED PERITONITIS. THE CAUSE OF PERITONITIS WAS UNKNOWN. THREE DAYS PRIOR TO THE RECEIPT OF THIS REPORT, THE PT WAS HOSPITALIZED FOR THE EVENT. THE PT RECEIVED TREATMENT FOR THE PERITONITIS WITH CEFTAZIDIME (1 GRAM, INTRAPERITONEALLY (IP) FOR 10 DAYS) AND VANCOMYCIN (500MG, IP, EVERY OTHER DAY FOR 10 DAYS). SIX DAYS AFTER BEING ADMITTED TO THE HOSPITAL, THE PT WAS DISCHARGED. AT THE TIME OF THIS REPORT, THE PATIENT HAD RECOVERED FROM THE EVENT AND DIANEAL THERAPIES WERE ONGOING. THIS IS REPORT 2 OF 3 INVOLVED IN THIS PERITONITIS EVENT.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
281513 MINICAP TRANSFER SET SET, ADMINISTRATION, FOR PERITONEAL DIALYSIS, DISPOSABLE KDJ BAXTER HEALTHCARE - MOUNTAIN HOME

Patients

Seq Age Sex Outcome Treatment
1 27 YR Hospitalization| R HOMECHOICE AUTOMATED PD SET WITH CASSETTE| DIANEAL PD4, 2.5% AMBUFLEX| MINICAP| DIANEAL PD4, 4.25% AMBUFLEX| DIANEAL PD4, 1.5% AMBUFLEX