Beckman Coulter Inc Cytomics FC 500 Flow Cytometry System with CXP Software Version 2.1 and 2.2 - FC 500 with UPS, Automated differential cell counter; Part Number: 626553; Beckman Coulter; Miami, FL 33196. Recall
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
Product
Cytomics FC 500 Flow Cytometry System with CXP Software Version 2.1 and 2.2 - FC 500 with UPS, Automated differential cell counter; Part Number: 626553; Beckman Coulter; Miami, FL 33196.
Brand
Beckman Coulter Inc
Lot Codes / Batch Numbers
Part Number 626553
Products Sold
Part Number 626553
Beckman Coulter Inc is recalling Cytomics FC 500 Flow Cytometry System with CXP Software Version 2.1 and 2.2 - FC 500 with UPS, Autom due to Incorrect Display: In certain modes, the protocol will not initially display the correct data in some plots. In addition, when running EWL files, any. Based on FDA medical device recall database.
Summary derived from FDA notice
Reason for Recall
As stated by FDA
Incorrect 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.
Recommended Action
Per FDA guidance
Consignees 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.
Verify this information on the official source
For complete details and official instructions, check the U.S. Food and Drug Administration (FDA) directly.
View official FDA recall noticePage updated: Jan 10, 2026