Beckman Coulter Inc CXP software, Part No. 623560, version 1.0 Recall
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
Product
CXP software, Part No. 623560, version 1.0
Brand
Beckman Coulter Inc
Lot Codes / Batch Numbers
Version 1.0
Products Sold
Version 1.0
Beckman Coulter Inc is recalling CXP software, Part No. 623560, version 1.0 due to Software anomaly. Sample ID and the Run Date may become fixed within a header on the FlowPAGE printout. All samples subsequently run, with results pri. Based on FDA medical device recall database.
Summary derived from FDA notice
Reason for Recall
As stated by FDA
Software anomaly. Sample ID and the Run Date may become fixed within a header on the FlowPAGE printout. All samples subsequently run, with results printed using the FlowPAGE print format, will have the fixed Sample ID and Run Date, rather than the correct Sample ID and Run Date.
Recommended Action
Per FDA guidance
Firm sent modified operating instructions to users on 13 February 2004.
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