Device recall
Z-1251-2025: human med Biofill Infiltration Cannula, diameter 2.5mm, 15cm, REF 2024-012, REF…
FDA device recall · Class II · HUMAN MED AG
Key facts
| Recall number (Z-number) | Z-1251-2025 |
|---|---|
| Recall event | 96137 |
| Product | human med Biofill Infiltration Cannula, diameter 2.5mm, 15cm, REF 2024-012, REF 1580107, sterile, single use. |
| Product code | QPB |
| Recalling firm | HUMAN MED AG |
| Recall class | Class II |
| Status | Open, Classified |
| 510(k) numbers | K082025 |
| FEI number | 3003587189 |
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