Device recall
Z-0961-2019: Alcon or Endure Ophthalmic Microscope Product Usage: Used for low magnification…
FDA device recall · Class II · Alcon Research Laboratories Ltd.
Key facts
| Recall number (Z-number) | Z-0961-2019 |
|---|---|
| Recall event | 82024 |
| Product | Alcon or Endure Ophthalmic Microscope Product Usage: Used for low magnification visualization during ophthalmic surgical procedures for cataract, retina and cornea. |
| Product code | HRM |
| Recalling firm | Alcon Research Laboratories Ltd. |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Apr 28, 2021 |
| FEI number | 1610287 |
At a glance
- None Linked 510(k)s
- 1–9 Products in the same recall event
- 1–9 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