FDA Adverse Event Malfunction Summary report: N

HOMECHOICE

MDR report key: 2233342 · Received September 2, 2011

Report

Report Number
1423500-2011-11657
Event Type
Malfunction
Date Received
September 2, 2011
Date of Event
May 4, 2009
Report Date
August 12, 2011
Manufacturer
BAXTER HEALTHCARE - LARGO
Product Code
FKX
PMA / PMN Number
K102936
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
FL, US
Reporter Occupation
OTHER

Narratives

Additional Manufacturer Narrative · 1

(B)(4). THE DEVICE HAS BEEN RECEIVED, AND THE EVALUATION IS IN PROCESS. A FOLLOW-UP MDR WILL BE SUBMITTED UPON COMPLETION OF THE EVALUATION OR IF ANY ADDITIONAL INFORMATION IS RECEIVED.

Additional Manufacturer Narrative · 1

(B)(4). THE DEVICE WAS RETURNED AND EVALUATED BY THE PRODUCT ANALYSIS LAB (PAL). THE PAL EVALUATED THE DEVICE AND NO FAILURE OR MALFUNCTION WAS IDENTIFIED THAT COULD HAVE CAUSED OR CONTRIBUTED TO THE INCREASED INTRA-PERITONEAL VOLUME (IIPV) FOUND IN THE DEVICE LOGS. DUE TO THE TEMPERATURE FAILURE DURING EVALUATION, IT IS UNKNOWN WHETHER THE DEVICE MET SPECIFICATIONS RELATIVE TO THE IIPVS FOUND IN THE DEVICE LOGS. THE CAUSE OF THE EVENT WAS UNDETERMINED, NOT ENOUGH INFORMATION WAS AVAILABLE TO MAKE A DETERMINATION.

Description of Event or Problem · 1

DURING INITIAL ASSESSMENT OF A RETURNED HOMECHOICE MACHINE, A BAXTER TECHNICIAN FOUND AN INCREASED INTRA-PERITONEAL VOLUME (IIPV) THAT WAS IDENTIFIED IN THE PATIENT THERAPY LOG WITH AN ULTRAFILTRATION OF 418 ML DURING CYCLE 1. THE FILL VOLUME WAS 200 ML. THERE WAS PATIENT INVOLVEMENT BUT NO PATIENT INJURY OR MEDICAL INTERVENTION INDICATED. THIS EVENT MEETS BAXTER'S OVERFILL CRITERIA. NO ADDITIONAL INFORMATION IS AVAILABLE.

Devices

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

Patients

Seq Age Sex Outcome Treatment
1