Device recall
Z-2247-2024: First Source iQ Flex M. Portable cart and platform that supports an X-ray system…
FDA device recall · Class II · First Source Inc
Key facts
| Recall number (Z-number) | Z-2247-2024 |
|---|---|
| Recall event | 94744 |
| Product | First Source iQ Flex M. Portable cart and platform that supports an X-ray system and laptop computer. |
| Product code | IZL |
| Recalling firm | First Source Inc |
| Recall class | Class II |
| Status | Open, Classified |
| 510(k) numbers | K221081 |
| FEI number | 3004063527 |
At a glance
- 1–9 Linked 510(k)s
- 1–9 Products in the same recall event
- 100–999 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