FDA Adverse Event Malfunction Summary report: N

CELL-DYN 22 CALIBRATOR

MDR report key: 789591 · Received December 1, 2006

Report

Report Number
2919069-2006-00106
Event Type
Malfunction
Date Received
December 1, 2006
Report Date
September 28, 2006
Manufacturer
ABBOTT DIAGNOSTICS DIV/CELLDYN
Product Code
KRZ
PMA / PMN Number
K902892/A
Removal / Correction Number
2919069-9/26/06-003-C
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
FL, US
Reporter Occupation
MEDICAL TECHNOLOGIST

Narratives

Additional Manufacturer Narrative · 1

ON-MARKET INSTABILITY FOR PLATELETS WITH CELL-DYN 22 CALIBRATOR LOTS 3098 AND 3099 IS BEING EXPERIENCED. THE CALIBRATOR COULD READK HIGHER BY AT LEAST 10% ON THE CELL-DYN RUBY AND AS MUCH AS 22% ON THE CELL-DYN 3200. IF THIS CALIBRATOR IS USED AND THE CALIBRATION FACTOR ON THE INSTRUMENT IS ADJUSTED, A NEGATIVE PLATELET SAMPLE BIAS COULD RESULT. AS A PRECAUTION, LOT 3100 WAS ALSO REMOVED FROM USE. INVESTIGATION INTO THE CAUSE OF THIS INSTABILITY IS IN PROGRESS. THIS IS AN INITIAL REPORT. AN INVESTIGATION IS IN PROCESS. A FINAL REPORT WILL BE SUBMITTED WHEN THE INVESTIGATION IS COMPLETE.

Description of Event or Problem · 1

THE ACCOUNT STATED THAT THEY HAD CALIBRATED THEIR CD3200 SL ANALYZER WITH CELL-DYN 22 CALIBRATOR LOT #'S 3099 AND 3100. THE ACCOUNT HAS BEEN GETTING DELTA CHECKS ON SOME PTS. DUE TO THE RECALL LETTER THAT THEY RECEIVED THEY ARE CONCERNED. THE CUSTOMER TECHNICAL ADVOCATE (CTA) SUGGESTED THAT THE ACCOUNT CHECK THE PT PLATELET VALUES WITH AN OUTSIDE LABORATORY. THE ACCOUNT DECLINED. THE ACCOUNT STATED THAT THEY HAVE NOT HAD ANY ISSUES WITH QC.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1 CELL-DYN 22 CALIBRATOR CD22 CALIBRATOR KRZ ABBOTT DIAGNOSTICS DIV/CELLDYN NA 3099 AND 3100

Patients

Seq Age Sex Outcome Treatment
1 NA CELL-DYN 3200 SL ANALYZER LIST # 4H60-01