COULTER LH 700 Series Hematology Analyzers
FDA device recall Z-0418-03 · posted 2003-01-09 · Terminated
Recall details
- Recalling firm
- Beckman Coulter Inc
- Reason for recall
- Software.
- Action taken
- Customers received a telephone call and a faxed Product Corrective Action letter dated Nov. 8, 2002 which includes modified operating instructions. Additionally an updated software version was released and installed on all affected customers units. This recall is complete.
- Root cause
- Other
- Status
- Terminated
- Product code
- GKZ
- Quantity affected
- 132
- Distribution
- Nationwide and Canada
- Date initiated
- 2002-11-08
- Date posted
- 2003-01-09
- Date terminated
- 2003-07-17
- Location
- Brea, CA
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