FDA Adverse Event Malfunction Summary report: N

HOMECHOICE AUTOMATED PD SET WITH CASSETTE

MDR report key: 2163543 · Received July 15, 2011

Report

Report Number
1423500-2011-09060
Event Type
Malfunction
Date Received
July 15, 2011
Date of Event
June 20, 2011
Report Date
June 20, 2011
Manufacturer
BAXTER HEALTHCARE - MOUNTAIN HOME
Product Code
FKX
PMA / PMN Number
K923065
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
US
Reporter Occupation
OTHER

Narratives

Additional Manufacturer Narrative · 1

(B)(4). THE COMPLAINT FOR SYSTEM ERROR 2240 WAS CONFIRMED, AND THE ROOT CAUSE WAS DETERMINED TO BE USE ERROR DUE TO THE PATIENT NOT BEING CONNECTED TO THE CYCLER WHEN ENTERING INITIAL DRAIN. A LABELING REVIEW OF THE HOMECHOICE APD SYSTEMS PATIENT AT-HOME GUIDE ISSUED WAS FOUND TO BE ADEQUATE FOR THE USE ERROR(S) IN THE COMPLAINT.

Additional Manufacturer Narrative · 1

(B)(4). THERE WAS NO ALLEGATION REPORTED AGAINST THE BAXTER PRODUCT BY THE CUSTOMER. THEREFORE THE DEVICE WAS NOT REQUESTED FOR EVALUATION AND A BATCH REVIEW WILL NOT BE CONDUCTED. A FOLLOW-UP REPORT WILL BE FILED UPON COMPLETION OF BAXTER'S INVESTIGATION, OR IF ANY ADDITIONAL INFORMATION IS RECEIVED.

Description of Event or Problem · 1

A CUSTOMER CONTACTED BAXTER GLOBAL TECHNICAL SERVICES REGARDING ASSISTANCE WITH A SYSTEM ERROR 2240 ALARM DURING THE INITIAL DRAIN ON THE HOMECHOICE MACHINE. THE HOME PATIENT (HP) STATED SHE PRESSED GO PRIOR TO CONNECTING. THE BAXTER TECHNICAL SERVICE REPRESENTATIVE (TSR) ASSISTED THE HP TO DISCONNECT AND CYCLE POWER. THE TSR ADVISED THE HP TO RESTART THE SETUP WITH ALL NEW SUPPLIES. THERE WAS PATIENT INVOLVEMENT; HOWEVER, THERE WAS NO INJURY OR MEDICAL INTERVENTION REPORTED.

Devices

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

Patients

Seq Age Sex Outcome Treatment
1 76 YR HOMECHOICE PRO