Device recall
Z-1075-2022: Digital Medical X-ray Imaging System, Model: uDR 596i, uDR 592h
FDA device recall · Class II · Shanghai United Imaging Healthcare Co., Ltd.
Key facts
| Recall number (Z-number) | Z-1075-2022 |
|---|---|
| Recall event | 90104 |
| Product | Digital Medical X-ray Imaging System, Model: uDR 596i, uDR 592h |
| Product code | KPR |
| Recalling firm | Shanghai United Imaging Healthcare Co., Ltd. |
| Recall class | Class II |
| Status | Terminated |
| Termination date | May 17, 2022 |
| 510(k) numbers | K181413 |
| FEI number | 3011015597 |
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