Customized Automation Centrifuge, First and Second Generation.
FDA device recall Z-0975-04 · posted 2004-07-20 · Terminated
Recall details
- Recalling firm
- Beckman Coulter Inc
- Reason for recall
- Centrifuge loss of containment with potential for injury or exposure to biohazard among lab workers.
- Action taken
- Recall was by letter and by telephone. All customers have been contacted.
- Root cause
- Other
- Status
- Terminated
- Product code
- JQC
- Quantity affected
- 17
- Distribution
- Nationwide
- Date initiated
- 2004-05-06
- Date posted
- 2004-07-20
- Date terminated
- 2004-11-30
- Location
- Brea, CA
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