FDA Adverse Event Malfunction Summary report: N

CD 3700 SL

MDR report key: 1080266 · Received July 22, 2008

Report

Report Number
2919069-2008-00639
Event Type
Malfunction
Date Received
July 22, 2008
Date of Event
June 27, 2008
Report Date
June 27, 2008
Manufacturer
ABBOTT DIAGNOSTICS DIVISION/CELLDYN
Product Code
GKZ
PMA / PMN Number
K980614
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
OK, US
Reporter Occupation
OTHER

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1 CD 3700 SL AUTOMATED HEMATOLOGY ANALYZER GKZ ABBOTT DIAGNOSTICS DIVISION/CELLDYN NA NA

Patients

Seq Age Sex Outcome Treatment
1 NI