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