Device recall
Z-1673-2014: Medrad Continuum MR Infusion system- non-wireless system The MEDRAD Continuum MR…
FDA device recall · Class II · Bayer Corp
Key facts
| Recall number (Z-number) | Z-1673-2014 |
|---|---|
| Recall event | 68293 |
| Product | Medrad Continuum MR Infusion system- non-wireless system The MEDRAD Continuum MR Infusion System is designed for patients who require medications and other fluids during an MR procedure. It is intended to provide infusion therapy directly prior to, during and immediately after the MR procedure… |
| Product code | FRN |
| Recalling firm | Bayer Corp |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Apr 16, 2015 |
| 510(k) numbers | K073051 |
| FEI number | 3010933360 |
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