Device recall
Z-1839-2021: NICO Myriad-LX Illumination Pack: REF: NN-1000 Mvriad-LX Illumination Pack. 11ga…
FDA device recall · Class II · Nico Corp.
Key facts
| Recall number (Z-number) | Z-1839-2021 |
|---|---|
| Recall event | 87882 |
| Product | NICO Myriad-LX Illumination Pack: REF: NN-1000 Mvriad-LX Illumination Pack. 11ga REF: NN-1001 Mvriad-LX Illumination Pack. l3ga Intended to perform resection and removal of soft tissues and fluids under direct visualization accessories to the NICO Myriad System. |
| Product code | GEI |
| Recalling firm | Nico Corp. |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Feb 5, 2024 |
| 510(k) numbers | K191599 |
| FEI number | 3007456622 |
At a glance
- 1–9 Linked 510(k)s
- 1–9 Products in the same recall event
- 100–999 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