Device recall
Z-1381-2023: NanoKnife 5-Probe Procedure Pack 15 cm - Activation. Indicated for the surgical…
FDA device recall · Class II · Angiodynamics, Inc.
Key facts
| Recall number (Z-number) | Z-1381-2023 |
|---|---|
| Recall event | 91909 |
| Product | NanoKnife 5-Probe Procedure Pack 15 cm - Activation. Indicated for the surgical ablation of soft tissue. Catalog Number: 20400111 UPN: H787204001110 |
| Product code | OAB |
| Recalling firm | Angiodynamics, Inc. |
| Recall class | Class II |
| Status | Open, Classified |
| 510(k) numbers | K183385 |
| FEI number | 1319211 |
At a glance
- 1–9 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