Device recall
Z-1093-04: SoFlex UV-Absorbing Model LI61U Silicone Posterior Chamber Intraocular Lens.
FDA device recall · Class II · Bausch & Lomb Surgical, Inc.
Key facts
| Recall number (Z-number) | Z-1093-04 |
|---|---|
| Recall event | 29055 |
| Product | SoFlex UV-Absorbing Model LI61U Silicone Posterior Chamber Intraocular Lens. |
| Product code | HQL |
| Recalling firm | Bausch & Lomb Surgical, Inc. |
| Recall class | Class II |
| Status | Terminated |
| Termination date | May 3, 2012 |
| FEI number | 1119279 |
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