Device recall
Z-0465-2022: Disposable Subdermal Needle Electrode, Corkscrew, Single Use, Sterile; Model…
FDA device recall · Class II · Technomed Europe
Key facts
| Recall number (Z-number) | Z-0465-2022 |
|---|---|
| Recall event | 89126 |
| Product | Disposable Subdermal Needle Electrode, Corkscrew, Single Use, Sterile; Model Numbers TE/S50715-001-C, TE/S50725-001C, and TE/S50715-001. |
| Product code | GXZ |
| Recalling firm | Technomed Europe |
| Recall class | Class II |
| Status | Terminated |
| Termination date | May 31, 2024 |
| 510(k) numbers | K130136 |
| FEI number | 3001450493 |
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