Device recall
Z-2890-2016: The EKOS cart has the catalog number 700-60101. The EKOS cart is a custom…
FDA device recall · Class II · EKOS Corporation
Key facts
| Recall number (Z-number) | Z-2890-2016 |
|---|---|
| Recall event | 75100 |
| Product | The EKOS cart has the catalog number 700-60101. The EKOS cart is a custom infusion stand/cart used to hold and transport the EkoSonic Control Unit. The cart is designed with three poles to hold infusion pumps and fluid bags, a tray on which the EkoSonic Control unit sits and a base designed to hold… |
| Product code | FOX |
| Recalling firm | EKOS Corporation |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Dec 30, 2016 |
| FEI number | 3001627457 |
At a glance
- None Linked 510(k)s
- 1–9 Products in the same recall event
- 1–9 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