FDA Adverse Event Injury Summary report: N

FLEXICAP

MDR report key: 3854794 · Received June 6, 2014

Report

Report Number
1416980-2014-18298
Event Type
Injury
Date Received
June 6, 2014
Date of Event
April 20, 2014
Report Date
May 13, 2014
Manufacturer
BAXTER HEALTHCARE - SWINFORD
Product Code
KDJ
PMA / PMN Number
K972579
Adverse Event
Yes
Report Source
Manufacturer report
Reporter Location
OR, US
Reporter Occupation
NURSE

Narratives

Additional Manufacturer Narrative · 1

(B)(4). A REVIEW OF ALL BATCH RECORD DOCUMENTS WAS PERFORMED FOR POTENTIALLY ASSOCIATED LOT NUMBER 13K14H25 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. SHOULD ADDITIONAL RELEVANT INFORMATION BECOME AVAILABLE, A SUPPLEMENTAL REPORT WILL BE SUBMITTED.

Additional Manufacturer Narrative · 1

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

Description of Event or Problem · 1

IT WAS REPORTED THAT A PATIENT EXPERIENCED PERITONITIS MANIFESTED BY STOMACH PAIN COINCIDENT WITH PERITONEAL DIALYSIS (PD) THERAPY. ON THE SAME DAY, THE PATIENT WAS HOSPITALIZED FOR THE EVENT, PD THERAPY WAS DISCONTINUED AND THE PATIENT STARTED HEMODIALYSIS (HD) THERAPY. DURING HOSPITALIZATION, THE PATIENT WAS TREATED WITH AN UNKNOWN ANTIBIOTIC (DOSE, ROUTE, FREQUENCY, AND DURATION NOT REPORTED) FOR PERITONITIS. ON AN UNKNOWN DATE, DURING HOSPITALIZATION, THE ANTIBIOTIC TREATMENT WAS DISCONTINUED. TEN DAYS AFTER HOSPITALIZATION, THE PATIENT WAS DISCHARGED. THE CAUSE OF PERITONITIS WAS NOT REPORTED. AT THE TIME OF THIS REPORT, THE EVENT OF PERITONITIS WAS ONGOING AND IMPROVED AND THE PATIENT WAS CONTINUING TO PERFORM HD THERAPY. NO ADDITIONAL INFORMATION IS AVAILABLE. THIS IS REPORT 3 OF 4.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
331273 FLEXICAP SET, ADMINISTRATION, FOR PERITONEAL DIALYSIS, DISPOSABLE KDJ BAXTER HEALTHCARE - SWINFORD

Patients

Seq Age Sex Outcome Treatment
1 59 YR Hospitalization| R CASSETTE, TRANSFER SET| DIANEAL PD4 AMBUFLEX, HOMECHOICE, MINICAP