FDA Adverse Event Malfunction Summary report: N

HOMECHOICE AUTOMATED PD SET WITH CASSETTE

MDR report key: 2983642 · Received February 28, 2013

Report

Report Number
1416980-2013-04980
Event Type
Malfunction
Date Received
February 28, 2013
Date of Event
February 4, 2013
Report Date
February 4, 2013
Manufacturer
BAXTER HEALTHCARE - MOUNTAIN HOME
Product Code
FKX
PMA / PMN Number
K923065
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
CA, US
Reporter Occupation
PATIENT

Narratives

Additional Manufacturer Narrative · 1

(B)(4). THIS IS REPORT IS THE SAME PATIENT AS (B)(4). THE REPORTED ISSUE WAS NOT CONFIRMED BECAUSE A SAMPLE WAS NOT RETURNED AND THE LOT NUMBER WAS UNKNOWN; HOWEVER THE CAUSE WAS DETERMINED TO BE USE ERROR AS IT WAS REPORTED THE TUBING WAS CUT. PER BAXTER LABELING, USERS ARE INSTRUCTED TO USE ASEPTIC TECHNIQUE WHEN PERFORMING PERITONEAL DIALYSIS. BY CUTTING THE TUBING ON THE CASSETTE, THERE WAS A BREACH IN THE STERILE FLUID PATHWAY. A FOLLOW-UP REPORT WILL BE SUBMITTED IF ADDITIONAL INFORMATION BECOMES AVAILABLE.

Description of Event or Problem · 1

IT WAS REPORTED THE PATIENT WAS SUPPOSED TO USE A HOMECHOICE AUTOMATED PD SET WITH 3-PRONG CASSETTE, BUT INSTEAD USED A HOMECHOICE AUTOMATED PD SET WITH 4-PRONG CASSETTE TO PERFORM PERITONEAL DIALYSIS (PD) THERAPY. THE PATIENT CUT THE TUBING ON THE CASSETTE AND TAPED THE TUBING TOGETHER AND CONTINUED TO USE THIS CASSETTE FOR PD THERAPY. THE HOME CARE SERVICE REPRESENTATIVE (HCSR) INSTRUCTED THE PATIENT TO DISCONTINUE USE OF THE INCORRECT/CUT CASSETTE AND NOTIFIED THE PD NURSE OF THE ISSUE. THERE WAS NO PATIENT INJURY OR MEDICAL INTERVENTION INDICATED AT THE TIME OF THE INITIAL REPORT. ADDITIONAL INFORMATION WAS REQUESTED, BUT WAS NOT AVAILABLE AT THIS TIME. THIS IS REPORT 2 OF 2.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
86647 HOMECHOICE AUTOMATED PD SET WITH CASSETTE SYSTEM, PERITONEAL, AUTOMATIC DELIVERY FKX BAXTER HEALTHCARE - MOUNTAIN HOME

Patients

Seq Age Sex Outcome Treatment
1