Device recall
Z-0557-2021: MANI TROCAR KIT 23G S - Product Usage: for use in injecting perfusate or…
FDA device recall · Class II · Mani, Inc. - Kiyohara Facility
Key facts
| Recall number (Z-number) | Z-0557-2021 |
|---|---|
| Recall event | 86873 |
| Product | MANI TROCAR KIT 23G S - Product Usage: for use in injecting perfusate or aspirating out intraocular materials during ophthalmic surgery, Ref: MTK 23S |
| Product code | NGY |
| Recalling firm | Mani, Inc. - Kiyohara Facility |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Aug 11, 2021 |
| 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