Device recall
Z-1140-2019: Foot Switches used with Philips MultiDiagnost Eleva with Flat Detector; Product…
FDA device recall · Class II · Philips Medical Systems Nederlands
Key facts
| Recall number (Z-number) | Z-1140-2019 |
|---|---|
| Recall event | 82459 |
| Product | Foot Switches used with Philips MultiDiagnost Eleva with Flat Detector; Product Codes: 708037, 708038 Product The Allura Xper FD Series are intended for use on human patients to perform: Vascular, cardiovascular and neurovascular imaging applications, including diagnostic, interventional and… |
| Product code | IZI |
| Recalling firm | Philips Medical Systems Nederlands |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Oct 14, 2020 |
| 510(k) numbers | K031333, K033737, K041949 |
| FEI number | 3002807880 |
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