Device recall
Z-2045-2016: Myriad handpiece Tissue morcellator
FDA device recall · Class II · Nico Corp.
Key facts
| Recall number (Z-number) | Z-2045-2016 |
|---|---|
| Recall event | 74191 |
| Product | Myriad handpiece Tissue morcellator |
| Product code | GEY |
| Recalling firm | Nico Corp. |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Jun 28, 2016 |
| 510(k) numbers | K955168 |
| FEI number | 3007456622 |
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