Device recall
Z-0283-2024: Philips EPIQ Diagnostic Ultrasound System Models: EPIQ 7G(model # 795200), EPIQ…
FDA device recall · Class II · Philips Ultrasound, Inc.
Key facts
| Recall number (Z-number) | Z-0283-2024 |
|---|---|
| Recall event | 93218 |
| Product | Philips EPIQ Diagnostic Ultrasound System Models: EPIQ 7G(model # 795200), EPIQ 7C (Model # 795201), EPIQ 7W (Model # 795202), EPIQ 5G (model # 795204), EPIQ 5W (model # 795206), EPIQ CVx (Model # 795231), EPIQ Elite (model # 795234) |
| Product code | IYN |
| Recalling firm | Philips Ultrasound, Inc. |
| Recall class | Class II |
| Status | Completed |
| 510(k) numbers | K231190 |
| FEI number | 3019216 |
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