Beckman Coulter Inc DL2000 Data Manager Software, Version 6.4.108 Recall
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
Product
DL2000 Data Manager Software, Version 6.4.108
Brand
Beckman Coulter Inc
Lot Codes / Batch Numbers
Version 6.4.108
Products Sold
Version 6.4.108
Beckman Coulter Inc is recalling DL2000 Data Manager Software, Version 6.4.108 due to Possibility of reporting an incorrect result occurs due to a software anomally.. Based on FDA medical device recall database.
Summary derived from FDA notice
Reason for Recall
As stated by FDA
Possibility of reporting an incorrect result occurs due to a software anomally.
Recommended Action
Per FDA guidance
Letters were sent to sites on November 5, 2004 to confirm previous telephone conversations with the consignees.
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 noticeDistribution
As reported by FDA
CA, FL, IL, IN
Page updated: Jan 10, 2026