Device recall
Z-0148-2023: sentec 24 / MARe-SF Multi-Site Attachment Ring Easy, For sensitive / fragile…
FDA device recall · Class II · SenTec AG
Key facts
| Recall number (Z-number) | Z-0148-2023 |
|---|---|
| Recall event | 90938 |
| Product | sentec 24 / MARe-SF Multi-Site Attachment Ring Easy, For sensitive / fragile skin. Used in continuous, noninvasive carbon dioxide and/or oxygen tension monitoring. |
| Product code | LKD |
| Recalling firm | SenTec AG |
| Recall class | Class II |
| Status | Terminated |
| Termination date | May 26, 2026 |
| 510(k) numbers | K151329 |
| FEI number | 3004149774 |
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