Device recall
Z-0804-2015: Radiomat M+ NIF 14 x 17, Radiomat M+ NIF 35CM x 43CM, Radiomat M+ NIF 10 x 12…
FDA device recall · Class III · AGFA Healthcare Corp.
Key facts
| Recall number (Z-number) | Z-0804-2015 |
|---|---|
| Recall event | 69864 |
| Product | Radiomat M+ NIF 14 x 17, Radiomat M+ NIF 35CM x 43CM, Radiomat M+ NIF 10 x 12, Radiomat M+ NIF 25,4CM x 30,5CM |
| Product code | IWZ |
| Recalling firm | AGFA Healthcare Corp. |
| Recall class | Class III |
| Status | Terminated |
| Termination date | Mar 16, 2015 |
| FEI number | 3001236302 |
At a glance
- None 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