Beckman Coulter Inc Synchron LX Systems Primary Tube Sample Template (a piece of ''labeling'' for use with the Synchron LX 20 and LX 20 Pro systems). Part Number: 967178 Recall
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
Product
Synchron LX Systems Primary Tube Sample Template (a piece of ''labeling'' for use with the Synchron LX 20 and LX 20 Pro systems). Part Number: 967178
Brand
Beckman Coulter Inc
Lot Codes / Batch Numbers
No range of serial numbers apply.
Products Sold
No range of serial numbers apply.
Beckman Coulter Inc is recalling Synchron LX Systems Primary Tube Sample Template (a piece of ''labeling'' for use with the Synchron due to Dead volume on sight gauge for the Synchron LX 20 and LX 20 Pro Systems not stated, which may result in instrument error.. Based on FDA medical device recall database.
Summary derived from FDA notice
Reason for Recall
As stated by FDA
Dead volume on sight gauge for the Synchron LX 20 and LX 20 Pro Systems not stated, which may result in instrument error.
Recommended Action
Per FDA guidance
A revised template with a recall letter was sent to customers with a response request on 19 June 2003.
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