FDA Adverse Event Malfunction Summary report: N

ACCESS® 2 IMMUNOASSAY ANALYZER

MDR report key: 2993706 · Received March 7, 2013

Report

Report Number
2122870-2013-00163
Event Type
Malfunction
Date Received
March 7, 2013
Date of Event
February 12, 2013
Report Date
February 12, 2013
Manufacturer
BECKMAN COULTER
Product Code
CDD
PMA / PMN Number
K922823/A007
Removal / Correction Number
NA
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
MI, US
Reporter Occupation
HEALTH PROFESSIONAL

Narratives

Additional Manufacturer Narrative · 1

A BECKMAN COULTER CUSTOMER TECHNICAL SUPPORT (CTS) ASSISTED THE CUSTOMER WITH TROUBLESHOOTING. THE CTS ADVISED CUSTOMER TO CHANGE THE SUBSTRATE PROBE, PRIME THE SYSTEM AND PERFORM ANOTHER SYSTEM CHECK. THE CUSTOMER OBTAINED A PASSING SYSTEM CHECK, AND STATED THAT THE SYSTEM WAS PERFORMING WITHIN THE LABORATORY'S ESTABLISHED QUALITY CONTROL RANGES. AFTER SUCCESSFUL TROUBLESHOOTING, THE CTS RECOMMENDED THE CUSTOMER TO REPEAT ANY PATIENT SAMPLES THAT HAD BEEN TESTED ON THE PREVIOUS TWO DAYS. REPORTS ON TOTAL EIGHT (8) PATIENTS' RESULTS WERE CORRECTED. THIS REPORT DOCUMENTS SEVEN (7) OF THE EIGHT PATIENTS' RESULTS, AND THE RELATED EVENT ON THE OTHER ONE PATIENT TESTED ON (B)(6) 2013 IS DOCUMENTED IN MDR # 2122870-2013-00162.

Description of Event or Problem · 1

A CUSTOMER REPORTED TO BECKMAN COULTER THAT THE ACCESS 2 IMMUNOASSAY ANALYZER GENERATED ERRONEOUSLY ELEVATED VITAMIN B12 RESULTS FOR SEVEN (7) PATIENTS ON (B)(6) 2013. REPEAT TESTING PERFORMED ON THE SAME ANALYZER ON (B)(6) 2013, AFTER TROUBLESHOOTING, PRODUCED LOWER RESULTS. THE INITIAL RESULTS WERE REPORTED OUT OF THE LABORATORY, AND LATER CORRECTED. THE CUSTOMER STATED THAT NO HARM TO THE PATIENT HAD BEEN REPORTED.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
96708 ACCESS® 2 IMMUNOASSAY ANALYZER ANALYZER, CHEMISTRY (PHOTOMETRIC, DISCRETE), FOR CLINICAL USE CDD BECKMAN COULTER ACCESS 2 NA

Patients

Seq Age Sex Outcome Treatment
1