ClearanceBrief
Recall Z-2017-2008 ยท GKZ Counter, Differential Cell

Beckman Coulter Inc

Cytomics FC 500 Flow Cytometry System with CXP Software Version 2.1 and 2.2 - FC 500 120V, Automated differential cell counter; Part Number 6605628; Beckman Coulter; Miami, FL 33196.

DateJul 11, 2008 (initiated May 4, 2007)
StatusTerminated
ReasonIncorrect Display: In certain modes, the protocol will not initially display the correct data in some plots. In addition, when running EWL files, any edited SampleID1 is not automatically updated in all tubes in the panel.
Root causeSoftware design
ActionConsignees were notified of this safety recall by an Urgent Product Corrective Action letter sent on 5/3/07. The letter provided instructions on how to ensure correct data acquisition. Users were requested to return a response form acknowledging receipt of the letter. For additional information contact 1-800-526-7694.
Quantity445 units in the US; 56 units in Canada
DistributionWorldwide Distribution including USA and country of Canada.
FDA recordOpen on fda.gov

510(k) clearances named in this recall

This recall record lists no 510(k) number.