Device recall
Z-0993-04: Fuji Flash IIP and CR-IR346CL Consoles
FDA device recall · Class III · Fujifilm Medical System USA, Inc.
Key facts
| Recall number (Z-number) | Z-0993-04 |
|---|---|
| Recall event | 29066 |
| Product | Fuji Flash IIP and CR-IR346CL Consoles |
| Product code | MQB |
| Recalling firm | Fujifilm Medical System USA, Inc. |
| Recall class | Class III |
| Status | Terminated |
| Termination date | Apr 20, 2005 |
| 510(k) numbers | K013218 |
| FEI number | 1000513161 |
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