Device recall
Z-0592-2019: IntelliVue MX40 Patient Monitor, Model Nos. 865350, 865351, 865352, 867146…
FDA device recall · Class II · Philips Electronics North America Corporation
Key facts
| Recall number (Z-number) | Z-0592-2019 |
|---|---|
| Recall event | 81531 |
| Product | IntelliVue MX40 Patient Monitor, Model Nos. 865350, 865351, 865352, 867146 - Product Usage: Indicated for use by health care professionals whenever there is a need for monitoring the physiological parameters of patients. Intended for monitoring and recording of, and to generate alarms for, multiple… |
| Product code | DSI |
| Recalling firm | Philips Electronics North America Corporation |
| 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