FDA Adverse Event Malfunction Summary report: N

UNICEL DXI 800 ACCESS IMMUNOASSAY SYSTEM

MDR report key: 2008330 · Received March 6, 2011

Report

Report Number
2122870-2011-00599
Event Type
Malfunction
Date Received
March 6, 2011
Date of Event
January 17, 2011
Report Date
February 3, 2011
Manufacturer
BECKMAN COULTER INC.
Product Code
JJE
PMA / PMN Number
K023764
Removal / Correction Number
N/A
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
AS
Reporter Occupation
OTHER

Narratives

Additional Manufacturer Narrative · 1

THE SAMPLE IS SERUM WHICH WAS CENTRIFUGED AUTOMATICALLY ON POWER PROCESSOR. QC AND/OR SYSTEM CHECK DATA WAS NOT PROVIDED. CUSTOMER IS NOT REPORTING ANY SYSTEM PERFORMANCE ISSUES. NO SYSTEM EVENT LOG MESSAGES REPORTED WITH THIS EVENT. DUE TO THE BELATED REPORTING OF THIS EVENT, SAMPLE WAS UNAVAILABLE FOR TESTING BY CUSTOMER PRODUCT LINE SUPPORT (CPLS). SERVICE WAS NOT DISPATCHED. HETEROPHILE INTERFERENCE IS THE LIKELY ROOT CAUSE FOR THIS EVENT.

Description of Event or Problem · 1

A CUSTOMER CONTACTED BECKMAN COULTER INC. (BCI) TO REPORT ERRONEOUSLY ELEVATED THYROID STIMULATING HORMONE (TSH) RESULT FOR A PATIENT GENERATED BY UNICEL DXI 800 ACCESS CHEMISTRY ANALYZER. THE RESULT WAS REPORTED OUT OF THE LABORATORY AND QUESTIONED BY THE PHYSICIAN SINCE IT DID NOT MATCH THE PATIENT'S CLINICAL PRESENTATION. THE SAMPLE WAS REPEATED WITH SCANTIBODIES HRT ON THE SAME UNIT AND LOWER RESULT WAS OBTAINED. IN ADDITION, THE SAMPLE WAS REPEATED ON ALTERNATE METHODOLOGY AT A REFERENCE LABORATORY AND A RESULT WITHIN NORMAL REFERENCE RANGE WAS OBTAINED. AMENDED REPORT WAS INITIATED AND SUBMITTED TO THE PHYSICIAN. THE CUSTOMER WAS NOT MADE AWARE OF ANY PATIENT INJURY OR CHANGE IN TREATMENT ASSOCIATED WITH EVENT.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1 UNICEL DXI 800 ACCESS IMMUNOASSAY SYSTEM DISCRETE PHOTOMETRIC CHEMISTRY ANALYZER JJE BECKMAN COULTER INC. DXI 800 N/A

Patients

Seq Age Sex Outcome Treatment
1