Device recall
Z-1468-2023: Mani Trocar Kit, Model MTK23S and Model MTK25S There are 3 kits contained in one…
FDA device recall · Class II · Mani, Inc. - Kiyohara Facility
Key facts
| Recall number (Z-number) | Z-1468-2023 |
|---|---|
| Recall event | 91829 |
| Product | Mani Trocar Kit, Model MTK23S and Model MTK25S There are 3 kits contained in one box, and sterile 1 kit consists of 3 pcs. trocar with the valved cannula and 1 pc. infusion cannula. |
| Product code | NGY |
| Recalling firm | Mani, Inc. - Kiyohara Facility |
| Recall class | Class II |
| Status | Terminated |
| Termination date | May 19, 2025 |
| FEI number | 3002692886 |
At a glance
- None 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