Device recall
Z-1445-2014: Alcon LenSx Ophthalmic Laser, for use in cataract surgery for the creation of…
FDA device recall · Class II · Alcon LenSx, Inc.
Key facts
| Recall number (Z-number) | Z-1445-2014 |
|---|---|
| Recall event | 67755 |
| Product | Alcon LenSx Ophthalmic Laser, for use in cataract surgery for the creation of corneal cuts/incisions, anterior capsulotomy and laser phacofragmentation. |
| Product code | OOE |
| Recalling firm | Alcon LenSx, Inc. |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Oct 16, 2014 |
| FEI number | 3008772169 |
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