Beckman Coulter Inc Coulter LH750 Hematology Analyzer. Part Number 6605632. Recall
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
Product
Coulter LH750 Hematology Analyzer. Part Number 6605632.
Brand
Beckman Coulter Inc
Lot Codes / Batch Numbers
Software versions 2A2 and 2B1.
Products Sold
Software versions 2A2 and 2B1.
Beckman Coulter Inc is recalling Coulter LH750 Hematology Analyzer. Part Number 6605632. due to If a customer enters a dilution factor for Sample B prior to the results from Sample A being transfered to the workstation, the predilute multiplicat. Based on FDA medical device recall database.
Summary derived from FDA notice
Reason for Recall
As stated by FDA
If a customer enters a dilution factor for Sample B prior to the results from Sample A being transfered to the workstation, the predilute multiplication factor will be applied erroneously to the Sample A's results once they are received at the workstation.
Recommended Action
Per FDA guidance
A Product Corrective Action Letter was mailed to all customers who currently have the instrument in thier lab. The letter includes a description of what conditions need to be met for the error to occur and the proper steps to prevent the issue from occuring. The letter was sent by US Mail on March 31, 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