Device recall
Z-0539-04: Collamer UV One-Piece IntraOcular Lens. Models 4205BF and 4204BF
FDA device recall · Class II · Staar Surgical Co Inc
Key facts
| Recall number (Z-number) | Z-0539-04 |
|---|---|
| Recall event | 28264 |
| Product | Collamer UV One-Piece IntraOcular Lens. Models 4205BF and 4204BF |
| Product code | HQL |
| Recalling firm | Staar Surgical Co Inc |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Jan 4, 2005 |
| 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