FDA Adverse Event Malfunction Summary report: N

UV-FLASH SOLUTION TRANSFER SET(SHORT) - JAPAN

MDR report key: 1873146 · Received October 18, 2010

Report

Report Number
1423500-2010-04570
Event Type
Malfunction
Date Received
October 18, 2010
Date of Event
September 27, 2010
Report Date
September 28, 2010
Manufacturer
BAXTER HEALTHCARE - MOUNTAIN HOME
Product Code
KDJ
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
JA
Reporter Occupation
NURSE

Narratives

Additional Manufacturer Narrative · 1

(B)(4). THE CUSTOMER REPORT OF A BENT SPIKE WAS CONFIRMED DURING EVALUATION OF THE TRANSFER SET. THE SET WAS VISUALLY INSPECTED WITH A BENT SPIKE OBSERVED. NO OTHER MANUFACTURING ABNORMALITIES WERE NOTED DURING VISUAL INSPECTION. PRESSURE TEST OF THE SAMPLE FOUND NO LEAKS. NO BATCH REVIEW COULD BE PERFORMED SINCE THE LOT NUMBER WAS UNKNOWN. THE ROOT CAUSE WAS UNDETERMINED. RENAL QUALITY ENGINEERING, ALONG WITH PLANT QUALITY AND MANUFACTURING PERSONNEL, WILL CONTINUE TO MONITOR THIS PRODUCT LINE FOR TRENDS AND WILL TAKE CORRECTIVE/PREVENTIVE ACTION AS APPROPRIATE.

Additional Manufacturer Narrative · 1

(B)(4). A 510(K) NUMBER WILL NOT BE PROVIDED IN THE EMDR AS THIS PRODUCT IS MANUFACTURED FOR DISTRIBUTION OUTSIDE OF THE U.S. AND DOES NOT HAVE A 510(K) NUMBER. HOWEVER, IT IS BEING REPORTED BECAUSE IT IS THE SAME AS OR SIMILAR TO PRODUCT DISTRIBUTED WITHIN THE U.S. THE SAMPLE HAS BEEN RECEIVED. A FOLLOW-UP REPORT WILL BE SUBMITTED UPON COMPLETION OF THE EVALUATION.

Description of Event or Problem · 1

THE CUSTOMER REPORTED THE SPIKE ON THE TRANSFER SET BENT WHILE CONNECTING TO THE YUME SET. THERE WAS NO PATIENT INJURY OR MEDICAL INTERVENTION. THE ACTUAL SAMPLE IS AVAILABLE FOR EVALUATION.

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