Device recall
Z-1273-2021: Philips CT systems are advanced continuous-rotation computed tomography systems…
FDA device recall · Class II · Philips Healthcare (Suzhou) Co., Ltd.
Key facts
| Recall number (Z-number) | Z-1273-2021 |
|---|---|
| Recall event | 87473 |
| Product | Philips CT systems are advanced continuous-rotation computed tomography systems suitable for a wide range of computed tomographic (CT) applications - Product Usage: intended for use in the head and whole body. |
| Product code | JAK |
| Recalling firm | Philips Healthcare (Suzhou) Co., Ltd. |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Feb 17, 2023 |
| 510(k) numbers | K180015 |
| FEI number | 3009529630 |
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