Device recall
Z-2096-2017: AMO 25GA Vitrectomy Cutter (Model Number NGP0025) and AMO 20GA Vitrectomy Cutter…
FDA device recall · Class II · Abbott Medical Optics Inc. (AMO)
Key facts
| Recall number (Z-number) | Z-2096-2017 |
|---|---|
| Recall event | 77024 |
| Product | AMO 25GA Vitrectomy Cutter (Model Number NGP0025) and AMO 20GA Vitrectomy Cutter and Irrigation Sleeve (Model Number NGP0020) Used with the AMO Whitestar Signature System. For ophthalmic use. |
| Product code | MLZ |
| Recalling firm | Abbott Medical Optics Inc. (AMO) |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Aug 23, 2017 |
| 510(k) numbers | K081681 |
| FEI number | 3003843509 |
At a glance
- 1–9 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