Device recall
Z-1695-2019: IntelliVue MX40 Patient Monitor, Product number 857146, Service Numbers All…
FDA device recall · Class II · Philips North America, LLC
Key facts
| Recall number (Z-number) | Z-1695-2019 |
|---|---|
| Recall event | 82696 |
| Product | IntelliVue MX40 Patient Monitor, Product number 857146, Service Numbers All: 453564711531 and 453564711541 - Product Usage: Used primarily as a traditional telemetry medical device. It connects to the IntelliVue Information Center by way of a wireless network. When the MX40 is connected to the… |
| Product code | DSI |
| Recalling firm | Philips North America, LLC |
| Recall class | Class II |
| Status | Open, Classified |
| 510(k) numbers | K113125 |
| FEI number | 1218950 |
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