FDA Adverse Event Malfunction Summary report: N

UNICEL® DXC 600I SYNCHRON® ACCESS CLINICAL SYSTEM

MDR report key: 2981806 · Received February 27, 2013

Report

Report Number
2122870-2013-00159
Event Type
Malfunction
Date Received
February 27, 2013
Date of Event
January 31, 2013
Report Date
February 1, 2013
Manufacturer
BECKMAN COULTER
Product Code
MMI
PMA / PMN Number
K060256
Removal / Correction Number
NA
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
IL, US
Reporter Occupation
HEALTH PROFESSIONAL

Narratives

Description of Event or Problem · 1

A CUSTOMER REPORTED TO BECKMAN COULTER THAT UNICEL DXC 600I SYNCHRON ACCESS CLINICAL SYSTEM GENERATED ERRATIC TROPONIN (ACCUTNI) RESULTS THAT WERE NOT REPRODUCIBLE FOR TOTAL OF 14 PATIENTS' SAMPLES DURING THE PERIOD OF (B)(6) 2013. THE ERRONEOUS RESULTS WERE NOT REPORTED OUT OF THE LABORATORY. THERE WAS NO REPORT OF DEATH, INJURY, OR CHANGE TO PATIENT TREATMENT ASSOCIATED TO THIS EVENT. BECKMAN COULTER FIELD SERVICE ENGINEER (FSE) VISITED THE CUSTOMER SITE ON (B)(6) 2013. THE FSE INSPECTED THE ANALYZER AND IDENTIFIED AN ISSUE WITH THE WASH PUMP AND WASH VALVE ALLOWING AIR TO ENTER THE FLUIDICS LINES. THE FSE REPLACED THE WASH PUMP SEAL, WASH VALVE STATOR AND SEAL. THE FSE PERFORMED A HIGH SENSITIVITY SYSTEM CHECK AND VERIFIED INSTRUMENT PERFORMANCE. ALL RESULTS WERE WITHIN THE SPECIFICATIONS. THE LIKELY CAUSE OF THE EVENTS WAS PREMATURE FAILURE OF COMPONENTS OF THE WASH PUMP AND WASH VALVE. THIS REPORT DOCUMENTS THE EVENT OCCURRED ON (B)(6) 2013 ON TWO PATIENT'S SAMPLES. THE RELATED EVENTS ARE DOCUMENTED IN THE BELOW LISTED MEDICAL DEVICE REPORTS: 2122870-2013-00155, 2122870-2013-00156, 2122870-2013-00157, 2122870-2013-00158, 2122870-2013-00167, 2122870-2013-00168, 2122870-2013-00169, 2122870-2013-00170, 2122870-2013-00171, 2122870-2013-00172, 2122870-2013-00173.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
83384 UNICEL® DXC 600I SYNCHRON® ACCESS CLINICAL SYSTEM ANALYZER, CHEMISTRY (PHOTOMETRIC, DISCRETE), FOR CLINICAL USE MMI BECKMAN COULTER DXC 600I NA

Patients

Seq Age Sex Outcome Treatment
1 38