Device recall
Z-0600-2013: Medrad(R) Continuum MR Infusion System Primary VSA Set Peristaltic Pump System…
FDA device recall · Class II · Medrad Inc
Key facts
| Recall number (Z-number) | Z-0600-2013 |
|---|---|
| Recall event | 61734 |
| Product | Medrad(R) Continuum MR Infusion System Primary VSA Set Peristaltic Pump System 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 functioning while either… |
| Product code | FPA |
| Recalling firm | Medrad Inc |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Aug 17, 2015 |
| 510(k) numbers | K051499 |
| FEI number | 2520313 |
At a glance
- 1–9 Linked 510(k)s
- 10–99 Products in the same recall event
- 1,000+ 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