Device recall
Z-1240-2015: The I-Cart is used to store, transport, and power video equipment used in…
FDA device recall · Class II · Richard Wolf Medical Instruments Corp.
Key facts
| Recall number (Z-number) | Z-1240-2015 |
|---|---|
| Recall event | 70220 |
| Product | The I-Cart is used to store, transport, and power video equipment used in medical procedures. |
| Product code | KMI |
| Recalling firm | Richard Wolf Medical Instruments Corp. |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Jul 31, 2017 |
| FEI number | 1418479 |
At a glance
- None Linked 510(k)s
- 1–9 Products in the same recall event
- 10–99 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