Device recall
Z-1078-03: ''Alcon Ladarwave CustomCornea Wavefront System'' Aberrometer software Version…
FDA device recall · Class II · Alcon Laboratories, Inc.
Key facts
| Recall number (Z-number) | Z-1078-03 |
|---|---|
| Recall event | 26816 |
| Product | ''Alcon Ladarwave CustomCornea Wavefront System'' Aberrometer software Version 7.91 |
| Recalling firm | Alcon Laboratories, Inc. |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Jan 20, 2010 |
| 510(k) numbers | K023249 |
| FEI number | 3000209733 |
At a glance
- 1–9 Linked 510(k)s
- 1–9 Products in the same recall event
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