FDA Device recall Z-1694-2019
IntelliVue MX40 Patient Monitor, Product number 865352, Service Numbers All: 453564262571, 453564262591, 453564615311, 453564615331, 453564…
- FDA Device
- Class II
- ongoing
- Published 2019-06-12
On 2019-06-12 the FDA classified a Class II recall of IntelliVue MX40 Patient Monitor, Product number 865352, Service Numbers All: 453564262571, 453564262591, 453564615311, 453564615331, 453564… by Philips North America, citing the MX40 may experience increased power consumption and may have a lack of visual and/or audible notifications while in a Low Battery State .
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-1694-2019 |
| Classification | Class II |
| Status | ongoing |
| Initiated | 2019-03-28 |
| Published | 2019-06-12 |
| Last updated | 2026-09-13 11:55 UTC |
| Company | Philips North America |
| Distribution | US |
Product
IntelliVue MX40 Patient Monitor, Product number 865352, Service Numbers All: 453564262571, 453564262591, 453564615311, 453564615331, 453564615351, and 453564615371 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 IntelliVue Information Center the IntelliVue Information Center provides the primary patient monitoring and alarming function. The MX40 does not automatically provide local monitoring or alarming when connected to the Information Center.
Reason
The MX40 may experience increased power consumption and may have a lack of visual and/or audible notifications while in a Low Battery State .
Identifiers
| code_info | All revision B.X versions are affected. |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:55 UTC. Current status: ongoing.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-1694-2019%22
RecallRadar indexes public recall notices from the FDA, USDA FSIS, and CPSC. The official agency notice is the authoritative source. Always confirm details at the linked source before acting.