Beckman Coulter Inc DL 2000 Data Manager, Software Version 6.2 Recall
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
Product
DL 2000 Data Manager, Software Version 6.2
Brand
Beckman Coulter Inc
Lot Codes / Batch Numbers
Version 6.2
Products Sold
Version 6.2
Beckman Coulter Inc is recalling DL 2000 Data Manager, Software Version 6.2 due to Software defect. The type of results affected were replicate type results for a single sample transmitted within the same data stream.. Based on FDA medical device recall database.
Summary derived from FDA notice
Reason for Recall
As stated by FDA
Software defect. The type of results affected were replicate type results for a single sample transmitted within the same data stream.
Recommended Action
Per FDA guidance
Recall is complete. Letters were mailed to customers on 2/14/2003. Instruments received upated software version 6.3.
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