Beckman Coulter Inc Synchron CX Systems version 4.0 Operating Software used in Synchron LX20 Systems, Synchron LX20 Pro Systems, Synchron LXi Systems. Recall
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
Product
Synchron CX Systems version 4.0 Operating Software used in Synchron LX20 Systems, Synchron LX20 Pro Systems, Synchron LXi Systems.
Brand
Beckman Coulter Inc
Lot Codes / Batch Numbers
All those with version 4.0 operating software.
Products Sold
All those with version 4.0 operating software.
Beckman Coulter Inc is recalling Synchron CX Systems version 4.0 Operating Software used in Synchron LX20 Systems, Synchron LX20 Pro due to Sample wheel may home to the wrong position.. Based on FDA medical device recall database.
Summary derived from FDA notice
Reason for Recall
As stated by FDA
Sample wheel may home to the wrong position.
Recommended Action
Per FDA guidance
Recall is accomplished by telephone and by letter. Telephone calls were made by 9/24/2003. All customers have been notified by telephone.
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