Device recall
Z-1506-2013: The Constellation Vision System Pneumatic Handpiece. Indicated for both anterior…
FDA device recall · Class II · Alcon Grieshaber AG
Key facts
| Recall number (Z-number) | Z-1506-2013 |
|---|---|
| Recall event | 65006 |
| Product | The Constellation Vision System Pneumatic Handpiece. Indicated for both anterior and posterior segment opthalmic surgery. |
| Product code | HQE |
| Recalling firm | Alcon Grieshaber AG |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Jan 7, 2015 |
| FEI number | 3003398873 |
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