Device recall
Z-0600-2026: NICO Myriad Illumination Pack Product No. NN-1000 11g Illumination Sleeve/Fiber…
FDA device recall · Class II · Stryker Corporation
Key facts
| Recall number (Z-number) | Z-0600-2026 |
|---|---|
| Recall event | 97833 |
| Product | NICO Myriad Illumination Pack Product No. NN-1000 11g Illumination Sleeve/Fiber; Product No. NN-1001 13g Illumination Sleeve/Fiber |
| Product code | GEI |
| Recalling firm | Stryker Corporation |
| Recall class | Class II |
| Status | Open, Classified |
| 510(k) numbers | K191599, K232567 |
| FEI number | 3015967359 |
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