OLA 2500 Olympus Lab Automation Systems to include the following models (all serial numbers): S2 Full Size, S3 Full Size
FDA device recall Z-0322-06 · posted 2005-12-23 · Terminated
Recall details
- Recalling firm
- Olympus America, Inc
- Reason for recall
- Lab Automation System may dilute samples with water.
- Action taken
- Firm initiated recall on 11/18/05 via letter to all direct accounts.
- Root cause
- Other
- Status
- Terminated
- Product code
- JQP
- Quantity affected
- 6 total units.
- Distribution
- Nationwide; Distribution was made to laboratories and blood centers located in CA, CO, GA, NC, and OH.
- Date initiated
- 2005-11-18
- Date posted
- 2005-12-23
- Date terminated
- 2008-03-10
- Location
- Irving, TX
Monitor recalls programmatically
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