FDA Adverse Event Injury Summary report: N

ACCESS® 2 IMMUNOASSAY CLINICAL SYSTEM

MDR report key: 2060356 · Received April 15, 2011

Report

Report Number
2122870-2011-01002
Event Type
Injury
Date Received
April 15, 2011
Date of Event
March 17, 2011
Report Date
March 17, 2011
Manufacturer
BECKMAN COULTER, INC.
Product Code
MMI
PMA / PMN Number
K922823/A007
Removal / Correction Number
NA
Adverse Event
Yes
Report Source
Manufacturer report
Reporter Location
CA, US
Reporter Occupation
OTHER

Narratives

Additional Manufacturer Narrative · 1

THE SAMPLE WAS COLLECTED IN A LITHIUM HEPARIN PLASMA TUBE WITH A GEL SEPARATOR. CENTRIFUGATION INFORMATION HAS NOT BEEN SUPPLIED TO DATE. QC IS PERFORMED ONCE EVERY 24 HOURS, AND WAS WITHIN THE ESTABLISHED RANGES PRIOR TO AND AFTER THE EVENT. A ROUTINE SYSTEM CHECK PERFORMED ON (B)(6) 2011 PASSED WITHIN INSTRUMENT SPECIFICATIONS. SERVICE WAS NOT DISPATCHED FOR THIS EVENT AS THE CUSTOMER HAS THEIR OWN BIO-MEDICAL ENGINEER (BME). BCI HAS MADE SEVERAL UNSUCCESSFUL ATTEMPTS TO CONTACT THE CUSTOMER FOR ADDITIONAL INFORMATION. HARDWARE VERIFICATION INFORMATION HAS NOT BEEN SUPPLIED TO DATE. A DEFINITIVE ROOT CAUSE HAS NOT BEEN DETERMINED TO DATE FOR THIS EVENT WITH THE DATA PROVIDED.

Description of Event or Problem · 1

A CUSTOMER CONTACTED BECKMAN COULTER, INC. (BCI) IN REGARDS TO AN ERRONEOUSLY ELEVATED TROPONIN (ACCUTNI) RESULT, ABOVE THE AMI CUTOFF, GENERATED BY ACCESS 2 IMMUNOASSAY SYSTEM FOR ONE PATIENT. THE RESULT WAS REPORTED OUT OF THE LABORATORY. SUBSEQUENT TESTING ON AN ALTERNATE INSTRUMENT PRODUCED A LOWER RESULT WITHIN THE NORMAL REFERENCE RANGE. THE PATIENT WAS TREATED WITH MEDICATION BUT THE SPECIFIC MEDICATION AND DOSAGE HAS NOT BEEN SUPPLIED TO DATE.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1 ACCESS® 2 IMMUNOASSAY CLINICAL SYSTEM DISCRETE PHOTOMETRIC CHEMISTRY ANALYZER MMI BECKMAN COULTER, INC. NA NA

Patients

Seq Age Sex Outcome Treatment
1 Other