Device recall
Z-0449-2021: Wuxi Nest, model numbers 202115, 202117, 202017, 202018 - Product Usage: Patient…
FDA device recall · Class II · Thomas Scientific
Key facts
| Recall number (Z-number) | Z-0449-2021 |
|---|---|
| Recall event | 86607 |
| Product | Wuxi Nest, model numbers 202115, 202117, 202017, 202018 - Product Usage: Patient specimen collection. |
| Product code | LIO |
| Recalling firm | Thomas Scientific |
| Recall class | Class II |
| Status | Open, Classified |
| FEI number | 2522600 |
At a glance
- None Linked 510(k)s
- 1–9 Products in the same recall event
- 1–9 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