FDA Adverse Event Malfunction Summary report: N

HOMECHOICE AUTOMATED PD SET WITH CASSETTE

MDR report key: 2233775 · Received September 3, 2011

Report

Report Number
1423500-2011-11667
Event Type
Malfunction
Date Received
September 3, 2011
Date of Event
August 15, 2011
Report Date
August 15, 2011
Manufacturer
BAXTER HEALTHCARE ? MOUNTAIN HOME
Product Code
FKX
PMA / PMN Number
K923065
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
AS
Reporter Occupation
OTHER

Narratives

Additional Manufacturer Narrative · 1

(B)(4). THIS COMPLAINT FOR THE SYSTEM ERROR 2240 CANNOT BE CONFIRMED AND THE ASSIGNABLE CAUSE WAS NOT DETERMINED. THE LOT NUMBER IS UNKNOWN; THEREFORE, A BATCH REVIEW CANNOT BE PERFORMED. BAXTER HAS CONDUCTED A TREND REVIEW AND FOUND THAT SIMILAR REPORTS HAVE BEEN RECEIVED FOR THE REPORTED PROBLEM. ADDITIONAL INVESTIGATION IS BEING CONDUCTED THROUGH (B)(4).

Additional Manufacturer Narrative · 1

(B)(4). 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'S TECHNICAL SERVICE CENTER REGARDING A SYSTEM ERROR (SE) 2240 (AIR IN LINE) ALARM THAT APPEARED ON THE HOMECHOICE (HC) DISPLAY DURING DWELL 3 OF 5. THE CARE GIVER (CG) STATED THAT THE HOME PATIENT (HP) IS STILL CONNECTED TO THE HC. THE TECHNICAL SERVICE REPRESENTATIVE (TSR) HAD THE CG CYCLE THE POWER TO PRESS GO TO START AND HAD THE CG DISCONNECT THE HP AND REMOVE THE CASSETTE TO DISCARD THE SUPPLIES. THE TSR EXPLAINED THE ALARM AND ASSISTED THE CG TO CLEAR THE ALARM AND ADVISED TO CONTACT THE NURSE. THERE WAS PATIENT INVOLVEMENT BUT NO PATIENT INJURY OR MEDICAL INTERVENTION WAS INDICATED AT THE TIME OF THE INITIAL REPORT.

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 HOMECHOICE