Device recall
Z-2706-2011: Brand Name STAAR Surgical Collamer Ultraviolet-Absorbing Posterior Chamber…
FDA device recall · Class II · Staar Surgical Co.
Key facts
| Recall number (Z-number) | Z-2706-2011 |
|---|---|
| Recall event | 59028 |
| Product | Brand Name STAAR Surgical Collamer Ultraviolet-Absorbing Posterior Chamber Single Piece Foldable Intraocular Lens Common Names Collamer single piece IOL Collamer plate haptic IOL The Device is intended to correct aphakia in persons 60 years of age or older in whom a cataractous lens has been removed… |
| Product code | HQL |
| Recalling firm | Staar Surgical Co. |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Mar 4, 2014 |
| PMA numbers | P990013 |
| FEI number | 2023826 |
At a glance
- None Linked 510(k)s
- 1–9 Products in the same recall event
- 10–99 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