FDA Adverse Event Malfunction Summary report: N

CELL-DYN EMERALD

MDR report key: 3130697 · Received May 24, 2013

Report

Report Number
2919069-2013-00047
Event Type
Malfunction
Date Received
May 24, 2013
Date of Event
March 27, 2013
Report Date
May 1, 2013
Manufacturer
ABBOTT DIAGNOSTICS DIVISION
Product Code
GKZ
PMA / PMN Number
K081495
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
US
Reporter Occupation
OTHER

Narratives

Additional Manufacturer Narrative · 1

(B)(4). PRODUCT EVALUATION IS IN PROCESS AND THE RESULTS WILL BE SUBMITTED IN A FOLLOW-UP REPORT.

Additional Manufacturer Narrative · 1

PRODUCT EVALUATION WAS PERFORMED IN ORDER TO INVESTIGATE THIS ISSUE. THE SYSMEX INSTRUMENT AND THE CD EMERALD HAVE FACTOR DIFFERENCES WHICH CAN AFFECT THEIR RESULTS, FOR EXAMPLES, DIFFERENT TECHNOLOGIES AND CALIBRATIONS OF EACH INSTRUMENT. THE INABILITY OF THE INSTRUMENT TO MEASURE A PARTICULAR MEASURE MAYBE DUE TO A SAMPLE ABNORMALITY. ANY SUBSTANCE OR CONDITION THAT CAN INTERFERE WITH THE CELL-DYN EMERALD SYSTEMS PRINCIPLES OF OPERATION SHOULD BE CONSIDERED AN INTERFERING SUBSTANCE OR CONDITION. BASED ON THE INVESTIGATION, THE CELL-DYN EMERALD ANALYZER WAS PERFORMING AS DESIGNED. THERE WAS NO PRODUCT DEFICIENCY, NO MALFUNCTION AND NO ACTION TAKEN FOR THE COMPLAINT ISSUE.

Description of Event or Problem · 1

THE CUSTOMER STATED THAT THE CELL DYN EMERALD ANALYZER GENERATED HIGHER PLT RESULTS FROM PATIENT SAMPLES COMPARED TO LOWER RESULTS GENERATED AT A REFERENCE LAB (QUEST). ONE PATIENT SAMPLE GENERATED A RESULT OF 29 K/UL ON THE CELL-DYN EMERALD AND A RESULT OF 19 AT THE REFERENCE LAB. THE SAME PATIENT WAS DRAWN ON (B)(6) 2013 AND A RESULT OF 43 K/UL WAS GENERATED ON THE EMERALD COMPARED TO A RESULT OF 19 GENERATED AT THE REFERENCE LAB. NO IMPACT TO PATIENT MANAGEMENT WAS REPORTED.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
230774 CELL-DYN EMERALD GKZ ABBOTT DIAGNOSTICS DIVISION

Patients

Seq Age Sex Outcome Treatment
1