Device recall
Z-1964-2016: STAAR AQ Cartridge-FP, guide and delivery system for Intraocular lenses.
FDA device recall · Class II · Staar Surgical Co.
Key facts
| Recall number (Z-number) | Z-1964-2016 |
|---|---|
| Recall event | 74067 |
| Product | STAAR AQ Cartridge-FP, guide and delivery system for Intraocular lenses. |
| Product code | KYB |
| Recalling firm | Staar Surgical Co. |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Nov 15, 2016 |
| 510(k) numbers | K940593 |
| FEI number | 2023826 |
At a glance
- 1–9 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