FDA Adverse Event Malfunction Summary report: N

HOMECHOICE AUTOMATED PD SET WITH CASSETTE

MDR report key: 2200528 · Received August 11, 2011

Report

Report Number
1423500-2011-10538
Event Type
Malfunction
Date Received
August 11, 2011
Date of Event
July 19, 2011
Report Date
July 19, 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 A SYSTEM ERROR 2240 (AIR IN LINE) WAS NOT CONFIRMED. THE ROOT CAUSE WAS UNDETERMINED. THE DEVICE WAS REQUESTED BUT WAS NOT AVAILABLE. THE LOT NUMBER WAS NOT AVAILABLE THEREFORE A BATCH REVIEW WILL NOT BE PERFORMED. A LABELING REVIEW WAS NOT COMPLETED BECAUSE NO USE ERROR WAS SUSPECTED. BAXTER HAS CONDUCTED A TREND REVIEW AND FOUND THAT SIMILAR REPORTS HAVE BEEN RECEIVED FOR THE REPORTED PROBLEM. THE ROOT CAUSE INVESTIGATION IS IN PROGRESS THROUGH (B)(4).

Additional Manufacturer Narrative · 1

(B)(4). SHOULD ANY ADDITIONAL INFORMATION BECOME AVAILABLE, A FOLLOW-UP REPORT WILL BE SUBMITTED.

Description of Event or Problem · 1

A CUSTOMER CONTACTED GLOBAL TECHNICAL SERVICE (GTS) REGARDING A SYSTEM ERROR 2240 (AIR IN LINE) ALARM THAT APPEARED ON THE HOME CHOICE (HC) DURING USE. GTS ASSISTED THE HOME PATIENT (HP) TO CLEAR THE ALARM BY CYCLING POWER. GTS ADVISED THE HP TO END THERAPY, AND REVIEWED PROPER PROCEDURES. PRODUCT SURVEILLANCE (PS) SPOKE WITH THE HP'S NURSE, WHO WAS NOT AWARE OF THE ALARM. THE NURSE SAID THE HP WAS VERY GOOD AT CONTACTING THE CLINIC WITH ANY PROBLEMS. PS SUGGESTED A REVIEW OF PROPER PROCEDURES. THE PATIENT WAS INVOLVED BUT THERE WAS NO SERIOUS 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 52 YR HOMECHOICE