MicroSTAAR Injector, MSI-PF Packed ten per box.
FDA device recall Z-0957-04 · posted 2004-07-20 · Terminated
Recall details
- Recalling firm
- Staar Surgical Co Inc
- Reason for recall
- Cracking of the distal end of the injector occurs during locking of the cartridge into the nose cone of the injector.
- Action taken
- Recall will be implemented by visits by company representatives.
- Root cause
- Other
- Status
- Terminated
- Product code
- KYB
- Quantity affected
- 124 boxes, 10 per box.
- Distribution
- Nationwide
- Date initiated
- 2004-04-21
- Date posted
- 2004-07-20
- Date terminated
- 2012-07-26
- Location
- Monrovia, CA
Monitor recalls programmatically
Recalls and clearances share one API, with change alerts when new recalls post.
Related 510(k) clearances
| Record | Firm | Date |
|---|---|---|
| FOAM TIP INJECTOR (K980696) | Staar Surgical Co. | 1998-09-11 |