Device recall
Z-1737-2022: Disposable Subdermal Needle Electrode, Pt/lr, 12 x 0.40mm, product number…
FDA device recall · Class II · Technomed Europe
Key facts
| Recall number (Z-number) | Z-1737-2022 |
|---|---|
| Recall event | 90733 |
| Product | Disposable Subdermal Needle Electrode, Pt/lr, 12 x 0.40mm, product number TE/S46/638, 25 needles per package, sterile. |
| Product code | IKT |
| Recalling firm | Technomed Europe |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Apr 11, 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
- 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