Device recall
Z-2438-2021: Solero Generator Refurbished PG, Item No. H78712740000D0, Catalog No. 12740000D
FDA device recall · Class II · Angiodynamics, Inc.
Key facts
| Recall number (Z-number) | Z-2438-2021 |
|---|---|
| Recall event | 88444 |
| Product | Solero Generator Refurbished PG, Item No. H78712740000D0, Catalog No. 12740000D |
| Product code | NEY |
| Recalling firm | Angiodynamics, Inc. |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Mar 15, 2023 |
| 510(k) numbers | K162449 |
| FEI number | 1319211 |
At a glance
- 1–9 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