Device recall
Z-1774-2013: PASCAL and PASCAL Streamline (532 nm.577 nm); Treats the patient's eye.
FDA device recall · Class II · Topcon Medical Laser Systems, Inc
Key facts
| Recall number (Z-number) | Z-1774-2013 |
|---|---|
| Recall event | 65688 |
| Product | PASCAL and PASCAL Streamline (532 nm.577 nm); Treats the patient's eye. |
| Product code | HQF |
| Recalling firm | Topcon Medical Laser Systems, Inc |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Jul 19, 2013 |
| 510(k) numbers | K100019 |
| FEI number | 2939653 |
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