FDA Adverse Event Malfunction Summary report: N

UV-FLASH SOLUTION TRANSFER SET(SHORT) - JAPAN

MDR report key: 1960615 · Received January 13, 2011

Report

Report Number
1423500-2011-00573
Event Type
Malfunction
Date Received
January 13, 2011
Date of Event
December 20, 2010
Report Date
December 20, 2010
Manufacturer
BAXTER HEALTHCARE - MOUNTAIN HOME
Product Code
KDJ
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
JA
Reporter Occupation
PHYSICIAN

Narratives

Additional Manufacturer Narrative · 1

(B)(4). ONE USED TRANSFER SET WAS RECEIVED WITH CAP ON SPIKE AND NO CAP ON PATIENT CONNECTOR IN REFERENCE TO LEAK. THE TRANSFER SET WAS TESTED UNDERWATER WITH LEAK NOTED FROM CUT APPROXIMATELY 4 5/8 FROM SLEEVE IN CLOSED POSITION. THIS REPORT OF A LEAK WAS CONFIRMED. A BATCH REVIEW WAS NOT PERFORMED AS LOT INFORMATION WAS UNKNOWN. BASED ON THE INFORMATION OBTAINED FROM BAXTER'S INVESTIGATION, THE ROOT CAUSE OF THIS REPORT WAS NOT DETERMINED. BAXTER WILL CONTINUE TO MONITOR SIMILAR REPORTS TO DETERMINE IF FURTHER ACTIONS ARE REQUIRED.

Additional Manufacturer Narrative · 1

(B)(4). THIS INTERNATIONAL PRODUCT IS DISTRIBUTED OUTSIDE THE U.S. AND DOES NOT HAVE A 510K NUMBER, BUT IT IS BEING REPORTED AS IT IS THE SAME OR SIMILAR TO A PRODUCT DISTRIBUTED WITHIN THE U.S. THE DEVICE HAS BEEN RECEIVED AND IS CURRENTLY BEING EVALUATED BY BAXTER. SHOULD ADDITIONAL INFORMATION BECOME AVAILABLE, A FOLLOW UP MDR WILL BE SENT.

Description of Event or Problem · 1

A CUSTOMER REPORTED TO BAXTER (B)(4) A LEAK FROM THE TRANSFER SET TUBING AFTER THE PATIENT TOOK A BATH. THERE WAS NO PATIENT INJURY OR MEDICAL INTERVENTION. THERE IS NO ADDITIONAL INFORMATION AVAILABLE.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1 UV-FLASH SOLUTION TRANSFER SET(SHORT) - JAPAN SET, ADMINISTRATION, FOR PERITONEAL DIALYSIS, DISPOSABLE KDJ BAXTER HEALTHCARE - MOUNTAIN HOME

Patients

Seq Age Sex Outcome Treatment
1 HOMECHOICE APD CYCLER