Device recall
Z-0810-2014: Medrad Veris MR Monitor units The system is intended to monitor physiological…
FDA device recall · Class II · Medrad Mr Inc
Key facts
| Recall number (Z-number) | Z-0810-2014 |
|---|---|
| Recall event | 66996 |
| Product | Medrad Veris MR Monitor units The system is intended to monitor physiological parameters of patients within any healthcare environment. The user, responsible to interpret the monitored data made available, will be a professional healthcare provider. Physiological data, gas monitoring, system alarms… |
| Product code | MWI |
| Recalling firm | Medrad Mr Inc |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Mar 30, 2015 |
| 510(k) numbers | K042569 |
| FEI number | 3006316319 |
At a glance
- 1–9 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