Device recall
Z-1470-2023: FujiFilm FDR AQRO (Model DR-XD1000)- A digital mobile X-ray system intended for…
FDA device recall · Class II · FUJIFILM Healthcare Americas Corporation
Key facts
| Recall number (Z-number) | Z-1470-2023 |
|---|---|
| Recall event | 92012 |
| Product | FujiFilm FDR AQRO (Model DR-XD1000)- A digital mobile X-ray system intended for use in general purpose radiography for generating radiographic images of human anatomy, including adult, pediatric, and neonatal exams |
| Product code | IZL |
| Recalling firm | FUJIFILM Healthcare Americas Corporation |
| Recall class | Class II |
| Status | Open, Classified |
| 510(k) numbers | K170858 |
| 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