FDA Adverse Event Malfunction Summary report: N

TRIMA ACCEL

MDR report key: 6029186 · Received October 14, 2016

Report

Report Number
1722028-2016-00562
Event Type
Malfunction
Date Received
October 14, 2016
Date of Event
September 19, 2016
Report Date
October 13, 2016
Manufacturer
TERUMO BCT
Product Code
GKT
PMA / PMN Number
BK150321
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
CA, US
Reporter Occupation
HEALTH PROFESSIONAL

Narratives

Additional Manufacturer Narrative · 1

INVESTIGATION: THE DEVICE HISTORY RECORDS (DHR) WERE REVIEWED FOR THIS LOT. THERE WERE NO EVENTS NOTED IN THE DHR THAT WOULD HAVE CONTRIBUTED TO THE ELEVATED WBC COUNT EXPERIENCED BY THE CUSTOMER. THE RUN DATA FILE (RDF) WAS ANALYZED FOR THIS EVENT. ROOT CAUSE: A DEFINITIVE ROOT CAUSE FOR THE OBSERVED LEUKOREDUCTION FAILURE REMAINS UNDETERMINED AT THIS TIME. THE ANALYSIS OF THE RUN DATA FILE DID NOT FIND A CONCLUSIVE CAUSE FOR THE HIGHER-THAN-EXPECTED WBC CONTENT REPORTED IN THE RBC PRODUCT FOR THIS COLLECTION. NO UNUSUAL PROCESS VARIABLE WAS IDENTIFIED AND THE SIGNALS IN THE RUN DATA FILE INDICATE THAT THE TRIMAACCEL SYSTEM OPERATED AS INTENDED. BASED ON THE AVAILABLE INFORMATION, IT IS POSSIBLE THAT THE FILTER WAS UNLOADED FROM THE FILTER BRACKET AND LOADED AGAIN DURING RBC COLLECTION OR RBC ADDITIVE SOLUTION ADDITION, WHICH COULD HAVE A SIMILAR AFFECT TO ¿SQUEEZING¿ THE FILTER WHEN USING A GRAVITY DRAIN SYSTEM. IT IS ALSO POSSIBLE THAT THE REPORTED RESULTS COULD BE ATTRIBUTED TO AN ISSUE WITH THE FILTER.

Description of Event or Problem · 1

THE CUSTOMER WOULD LIKE THE RUN DATA FILE INVESTIGATED TO DETERMINE A POSSIBLE CAUSE FOR THE ELEVATED WHITE BLOOD CELL (WBC) CONTENT IN THE RED BLOOD CELL (RBC) PRODUCT. THERE WAS NOT A TRANSFUSION RECIPIENT OR PATIENT INVOLVED AT THE TIME OF THE RESIDUAL WHITE BLOODCELL (RWBC) TESTING, THEREFORE NO PATIENT INFORMATION IS REASONABLY KNOWN AT THE TIME OF THE EVENT. DONOR UNIT #: (B)(6). THE RBC COLLECT SET IS NOT AVAILABLE FOR RETURN BECAUSE IT WAS DISCARDED BY THE CUSTOMER.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
681043 TRIMA ACCEL TRIMA ACCEL LRS PLT +35ML SAMPLER, PL, AUTORBC SET GKT TERUMO BCT 07Z3111

Patients

Seq Age Sex Outcome Treatment
1 Other