Device recall
Z-0742-2013: Mindray DPM5 Monitor, a vital signs monitor used on human patients in healthcare…
FDA device recall · Class II · Mindray DS USA, Inc. d.b.a. Mindray North America
Key facts
| Recall number (Z-number) | Z-0742-2013 |
|---|---|
| Recall event | 63800 |
| Product | Mindray DPM5 Monitor, a vital signs monitor used on human patients in healthcare facilities. |
| Product code | MWI |
| Recalling firm | Mindray DS USA, Inc. d.b.a. Mindray North America |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Oct 22, 2013 |
| 510(k) numbers | K053234 |
| FEI number | 2221819 |
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