FDA Adverse Event Malfunction Summary report: N

HOMECHOICE AUTOMATED PD SET WITH CASSETTE

MDR report key: 3251582 · Received July 29, 2013

Report

Report Number
1416980-2013-19996
Event Type
Malfunction
Date Received
July 29, 2013
Date of Event
July 3, 2013
Report Date
July 4, 2013
Manufacturer
BAXTER HEALTHCARE - MOUNTAIN HOME
Product Code
FKX
PMA / PMN Number
K923065
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
CA
Reporter Occupation
OTHER

Narratives

Additional Manufacturer Narrative · 1

(B)(4). AN ALARM INDICATIVE OF A POTENTIAL MALFUNCTION OF THE DISPOSABLE CASSETTE WAS IDENTIFIED. AS THE CASSETTE WAS NOT RETURNED AND THE LOT NUMBER IS UNKNOWN, A DEVICE ANALYSIS CANNOT BE COMPLETED. SHOULD ADDITIONAL RELEVANT INFORMATION BECOME AVAILABLE, A SUPPLEMENTAL REPORT WILL BE SUBMITTED.

Description of Event or Problem · 1

IT WAS REPORTED THAT WHILE PERFORMING PERITONEAL DIALYSIS, A HOME PATIENT (HP) HAD RECEIVED A SYSTEM ERROR 2240 (AIR IN SET) ALARM ON A HOMECHOICE (HC) MACHINE DURING PATIENT USE. THE ALARM HAD OCCURRED THE NIGHT PRIOR TO THE CALL. THE CAREGIVER (CG) HAD SETUP THE HC FOR THERAPY FOR THE HP PRIOR TO LEAVING FOR WORK. AT AN UNKNOWN PART OF THERAPY, THE HC ALARMED. THE HP TRIED TO CLEAR THE ALARM BY CYCLING THE POWER BUT WAS NOT ABLE TO GET PAST PRIME AS THERE WAS AT LEAST ONE EMPTY BAG. THERE WAS NOTHING FOUND WITH THE SETUP DURING TROUBLESHOOTING THAT WOULD CAUSE OR CONTRIBUTE TO THE ALARM. THE TECHNICAL SERVICE REPRESENTATIVE (TSR) EXPLAINED THE ALARM TO THE CG AND ADVISED THAT THE HP SHOULD CALL AT THE TIME OF THE ALARM. NO PATIENT INJURY OR MEDICAL INTERVENTION WAS INDICATED IN ASSOCIATION WITH THIS REPORT. NO ADDITIONAL INFORMATION IS AVAILABLE.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
352826 HOMECHOICE AUTOMATED PD SET WITH CASSETTE SYSTEM, PERITONEAL, AUTOMATIC DELIVERY FKX BAXTER HEALTHCARE - MOUNTAIN HOME

Patients

Seq Age Sex Outcome Treatment
1 HOMECHOICE