Device recall
Z-0783-2024: EliA GBM Wells, Material Number 14551401, for Phadia 250, 2500, and 5000. In…
FDA device recall · Class II · Phadia Ab
Key facts
| Recall number (Z-number) | Z-0783-2024 |
|---|---|
| Recall event | 93403 |
| Product | EliA GBM Wells, Material Number 14551401, for Phadia 250, 2500, and 5000. In vitro diagnostic |
| Product code | MOB |
| Recalling firm | Phadia Ab |
| Recall class | Class II |
| Status | Open, Classified |
| 510(k) numbers | K140225, K173792 |
| FEI number | 3002807876 |
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