FDA Adverse Event Malfunction Summary report: N

HOMECHOICE AUTOMATED PD SET WITH CASSETTE

MDR report key: 3070828 · Received April 22, 2013

Report

Report Number
1416980-2013-09991
Event Type
Malfunction
Date Received
April 22, 2013
Date of Event
April 13, 2013
Report Date
April 13, 2013
Manufacturer
BAXTER HEALTHCARE - MOUNTAIN HOME
Product Code
FKX
PMA / PMN Number
K923065
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
IA, US
Reporter Occupation
NURSE

Narratives

Additional Manufacturer Narrative · 1

(B)(4). THE SAMPLE WAS NOT AVAILABLE AND THE LOT NUMBER WAS UNKNOWN; THEREFORE, NO EVALUATION OR BATCH REVIEW COULD BE PERFORMED. A FOLLOW-UP REPORT WILL BE FILED IF ANY ADDITIONAL RELEVANT INFORMATION BECOMES AVAILABLE. PER BAXTER LABELING, USERS ARE INSTRUCTED TO NOT REPLACE EMPTY SOLUTION BAGS OR RECONNECT DISCONNECTED SOLUTION BAGS WHEN PERFORMING PERITONEAL DIALYSIS THERAPY. A REVIEW OF THE LABEL FOR THE PRODUCT FAMILY WILL BE CONDUCTED. IF THERE IS ANY FURTHER RELEVANT INFORMATION FROM THAT REVIEW, A SUPPLEMENTAL MEDWATCH WILL BE FILED.

Description of Event or Problem · 1

THE CUSTOMER CONTACTED BAXTER'S SERVICE CENTER DURING USE. THE REGISTERED NURSE (RN) STATED THAT THE HOME PATIENT (HP) RAN SHORT ON SOLUTION, SO THE RN DISCONNECTED AND RECONNECTED A NEW THE SUPPLY BAG. THE TECHNICAL SERVICE REPRESENTATIVE (TSR) ADVISED THE RN ONCE THE HC WAS PRIMED, YOU CAN NOT DISCONNECT AND RECONNECT THE SUPPLY BAG TO THE HEATER LINE. THE TSR ASSISTED THE RN END THERAPY. THE RN WOULD DO A MANUAL EXCHANGE. THERE WAS PATIENT INVOLVEMENT, BUT NO PATIENT INJURY OR MEDICAL INTERVENTION INDICATED AT THE TIME OF THE INITIAL REPORT.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
172438 HOMECHOICE AUTOMATED PD SET WITH CASSETTE SYSTEM, PERITONEAL, AUTOMATIC DELIVERY FKX BAXTER HEALTHCARE - MOUNTAIN HOME

Patients

Seq Age Sex Outcome Treatment
1 79 YR HOMECHOICE