Device recall
Z-2097-2021: Illuminated Stepped Laser Probe Curved-for use in combination with 23G…
FDA device recall · Class II · Dutch Ophthalmic USA, Inc.
Key facts
| Recall number (Z-number) | Z-2097-2021 |
|---|---|
| Recall event | 88146 |
| Product | Illuminated Stepped Laser Probe Curved-for use in combination with 23G vitrectomy system Product Code: 7510.ALC |
| Product code | HQF |
| Recalling firm | Dutch Ophthalmic USA, Inc. |
| Recall class | Class II |
| Status | Open, Classified |
| 510(k) numbers | K031023 |
| FEI number | 3007916166 |
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