Beckman Coulter Inc Cytomics FC500 with CXP Software Recall
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
Product
Cytomics FC500 with CXP Software
Brand
Beckman Coulter Inc
Lot Codes / Batch Numbers
Part Numbers 629636 629637
Products Sold
Part Numbers 629636 629637
Beckman Coulter Inc is recalling Cytomics FC500 with CXP Software due to Under certain conditions an incorrect Tube ID (Barcode) can be displayed and printed on the Runtime Panel Report in CXP Cytometer Software Version 2.0. Based on FDA medical device recall database.
Summary derived from FDA notice
Reason for Recall
As stated by FDA
Under certain conditions an incorrect Tube ID (Barcode) can be displayed and printed on the Runtime Panel Report in CXP Cytometer Software Version 2.0
Recommended Action
Per FDA guidance
A Product Corrective Action letter will be mailed the week of Nov 28, 2005 to all FC500 wi CXP Software customers. Each user will be contacted initially and then once more (if needed) in order to determine the rate of response from the Response form provided.
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