Device recall
Z-0854-2007: LADAR6000 Excimer Laser System
FDA device recall · Class I · Alcon Refractive Horizons, Inc.
Key facts
| Recall number (Z-number) | Z-0854-2007 |
|---|---|
| Recall event | 37605 |
| Product | LADAR6000 Excimer Laser System |
| Product code | LZS |
| Recalling firm | Alcon Refractive Horizons, Inc. |
| Recall class | Class I |
| Status | Terminated |
| Termination date | Mar 21, 2017 |
| PMA numbers | P970043 |
| FEI number | 3000209733 |
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