FDA Adverse Event Malfunction Summary report: N

HOMECHOICE PRO

MDR report key: 3031719 · Received April 2, 2013

Report

Report Number
1416980-2013-08188
Event Type
Malfunction
Date Received
April 2, 2013
Date of Event
December 10, 2012
Report Date
March 11, 2013
Manufacturer
BAXTER HEALTHCARE - LARGO
Product Code
FKX
Removal / Correction Number
1423500-01/08/10-001-C
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
TU
Reporter Occupation
PATIENT

Narratives

Additional Manufacturer Narrative · 1

(B)(4). THE DEVICE WAS RETURNED TO BAXTER, AND THE EVALUATION IS COMPLETE. THIS COMPLAINT IS AN ANCILLARY SERVICE EVENT. THE REPORTED DIFFICULTY OF AN IIPV EVENT WAS CONFIRMED THROUGH AN EVENT HISTORY LOG REVIEW. THE CAUSE WAS USE ERROR, INAPPROPRIATE BYPASS OF THE INITIAL DRAIN WITHOUT LOW DRAIN VOLUME ALARM OCCURRING. HOMECHOICE AND HOMECHOICE PRO APD SYSTEMS PATIENT AT-HOME GUIDE GIVES INSTRUCTIONS ON HOW TO BYPASS INITIAL DRAIN AND STATES "CONTACT YOUR DIALYSIS CENTER TO LEARN WHEN IT IS SAFE TO BYPASS." PAGE 18-37 ALSO HAS THE WARNING: "BYPASSING AN INITIAL DRAIN WHEN THERE IS STILL FLUID LEFT IN THE PERITONEAL CAVITY CAN RESULT IN AN INCREASED INTRAPERITONEAL VOLUME (IIPV) SITUATION LATER IN YOUR THERAPY. CHANGE YOUR POSITION OR SIT UP TO AID DRAINING COMPLETELY DURING THE INITIAL DRAIN." IF ANY ADDITIONAL INFORMATION IS RECEIVED, A FOLLOW-UP WILL BE SENT.

Description of Event or Problem · 1

DURING EVALUATION OF A RETURNED HOMECHOICE MACHINE, ONE INCREASED INTRA-PERITONEAL VOLUME (IIPV) EVENT WAS IDENTIFIED WHICH OCCURRED IN THE THERAPY INITIATED ON (B)(6) 2012 09:53:04. DURING NIGHT DRAIN CYCLE ONE, THE PATIENT'S ULTRAFILTRATION READING WAS 123ML, INDICATING THE HOME PATIENT (HP) DRAINED 123ML MORE THAN THEIR MAXIMUM PROGRAMMED FILL VOLUME OF 120ML. THIS INFORMATION MEETS IIPV CRITERIA. NO ADDITIONAL INFORMATION IS AVAILABLE.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
134495 HOMECHOICE PRO SYSTEM, PERITONEAL, AUTOMATIC DELIVERY FKX BAXTER HEALTHCARE - LARGO

Patients

Seq Age Sex Outcome Treatment
1