Device recall
Z-0988-2015: Femto LDV Z-Generation Femtosecond Surgical Lasers are used to perform…
FDA device recall · Class II · Ziemer Usa Inc
Key facts
| Recall number (Z-number) | Z-0988-2015 |
|---|---|
| Recall event | 70024 |
| Product | Femto LDV Z-Generation Femtosecond Surgical Lasers are used to perform ophthalmic surgeries. |
| Product code | HQF |
| Recalling firm | Ziemer Usa Inc |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Feb 20, 2018 |
| 510(k) numbers | K131207 |
| FEI number | 3006231532 |
At a glance
- 1–9 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