DL2000 Data Manager Software, Version 6.4.108
FDA device recall Z-0267-05 · posted 2004-11-30 · Terminated
Recall details
- Recalling firm
- Beckman Coulter Inc
- Reason for recall
- Possibility of reporting an incorrect result occurs due to a software anomally.
- Action taken
- Letters were sent to sites on November 5, 2004 to confirm previous telephone conversations with the consignees.
- Root cause
- Other
- Status
- Terminated
- Product code
- JQP
- Quantity affected
- 3
- Distribution
- Product was under evaluation at three sites in FL, IL, and CA.
- Date initiated
- 2004-11-05
- Date posted
- 2004-11-30
- Date terminated
- 2005-03-16
- Location
- Brea, CA
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