Device recall
Z-1693-2019: IntelliVue MX40 Patient Monitor, Product number 865351, Service Numbers All…
FDA device recall · Class II · Philips North America, LLC
Key facts
| Recall number (Z-number) | Z-1693-2019 |
|---|---|
| Recall event | 82696 |
| Product | IntelliVue MX40 Patient Monitor, Product number 865351, Service Numbers All other countries: 453564451791, 453564451811, 453564467721, 453564467741, 453564467761, 453564467781, 453564467801, 453564467821, 453564467841, 453564467861, 453564262531, and 453564262551 - Product Usage: Used primarily as a… |
| 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