Device recall
Z-0378-04: MicroSTAAR Injector Cartridges Models: SFC-25 (utilized with plate haptic…
FDA device recall · Class II · Staar Surgical Co Inc
Key facts
| Recall number (Z-number) | Z-0378-04 |
|---|---|
| Recall event | 28070 |
| Product | MicroSTAAR Injector Cartridges Models: SFC-25 (utilized with plate haptic Collamer lens) MTC-60 (utilized with plate haptic Silicone lens) |
| Product code | KYB |
| Recalling firm | Staar Surgical Co Inc |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Jan 4, 2005 |
| FEI number | 2023826 |
At a glance
- None Linked 510(k)s
- 1–9 Products in the same recall event
- 1–9 Recalled products with this product code
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About FDA device recalls (products)
Each recalled device product receives a Z-number. Recall details such as root cause, distribution and firm actions are available in Orca1.
Source: U.S. Food and Drug Administration (FDA), Medical Device Recalls database