Device recall
Z-1893-2019: Disposable 25GA Vitrectomy Cutter, REF NGP0025, RX Only, Abbott Medical Optics…
FDA device recall · Class II · Johnson & Johnson Surgical Vision Inc
Key facts
| Recall number (Z-number) | Z-1893-2019 |
|---|---|
| Recall event | 82868 |
| Product | Disposable 25GA Vitrectomy Cutter, REF NGP0025, RX Only, Abbott Medical Optics Inc., The product provides the item necessary to perform one vitrectomy procedure. It is used to remove vitreous from the eye. It has been designed as a disposable (single use) |
| Product code | MLZ |
| Recalling firm | Johnson & Johnson Surgical Vision Inc |
| Recall class | Class II |
| Status | Terminated |
| 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