DL2000 Data Manager Software, Version 6.4.108
FDA Recall Z-0267-05 · Posted 2004-11-30
Recalling FirmBeckman Coulter Inc
Recall StatusTerminated
Product CodeJQP
Date Initiated2004-11-05
Date Terminated2005-03-16
Product Quantity3
Reason for Recall
Possibility of reporting an incorrect result occurs due to a software anomally.
Firm Action
Letters were sent to sites on November 5, 2004 to confirm previous telephone conversations with the consignees.
Root Cause
Other
Distribution Pattern
Product was under evaluation at three sites in FL, IL, and CA.
Official Source
View FDA Recall →Source: FDA Enforcement Report / Recall database. Always confirm against the official FDA record.