FDA Adverse Event Malfunction Summary report: N

MINICAP EXTEND LIFE PD TRANSFSET W/TWIST CLAMP

MDR report key: 1193170 · Received October 7, 2008

Report

Report Number
1423500-2008-00859
Event Type
Malfunction
Date Received
October 7, 2008
Date of Event
August 7, 2008
Report Date
August 12, 2008
Manufacturer
BAXTER HEALTHCARE
Product Code
KDJ
PMA / PMN Number
K842885A
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
SF
Reporter Occupation
OTHER

Narratives

Additional Manufacturer Narrative · 1

EVALUATION SUMMARY: RESULTS INDICATE CONFIRMATION OF THE REPORTED EVENT OF A TRANSFER SET'S WHITE AND BLUE PART NOT CLICKING, AND IT'S PLASTIC PEELING OFF. ONE BROKEN OCCLUDER FOOT WAS FOUND DURING EVALUATION. A LIKELY ROOT CAUSE IS THE USE OF ENVIRONMENTAL STRESS CRACKING AGENTS (I.E., CHEMICAL SOLUTIONS IN CONTACT WITH THE PART UNDER AN APPLIED STRESS). RENAL QUALITY ENGINEERING, PLANT MANUFACTURING, AND QUALITY PERSONNEL WILL CONTINUE TO MONITOR THIS PRODUCT FOR TRENDS, AND TAKE CORRECTIVE/PREVENTIVE ACTION AS APPROPRIATE.

Description of Event or Problem · 1

A DISTRIBUTOR REPORTED TO BAXTER THAT A CUSTOMER COMPLAINED THAT A TRANSFER SET'S WHITE AND BLUE PART DOES NOT CLICK ANYMORE, AND THE PLASTIC IS PEELING OFF. NO INJURY OR MEDICAL INTERVENTION WAS REPORTED.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1 MINICAP EXTEND LIFE PD TRANSFSET W/TWIST CLAMP 78KDJ KDJ BAXTER HEALTHCARE H07K14044

Patients

Seq Age Sex Outcome Treatment
1