MicroSTAAR Injector w/ Foam Tip Plunger, Model MSI-PF
FDA device recall Z-0766-04 · posted 2004-07-20 · Terminated
Recall details
- Recalling firm
- Staar Surgical Co Inc
- Reason for recall
- Injector mold design/manufacture and wear caused material flash to develop preventing assembly of the device prior to use.
- Action taken
- Firm will be sending thier representatives to customers to inspect inventory and arrange return of product.
- Root cause
- Other
- Status
- Terminated
- Product code
- KYB
- Quantity affected
- 690 injectors
- Distribution
- Nationwide.
- Date initiated
- 2004-02-23
- Date posted
- 2004-07-20
- Date terminated
- 2005-01-04
- Location
- Monrovia, CA
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