IntelliVue MX40 Patient Monitor — Class II medical device recall Z-1695-2019
Ongoing recall by Philips North America, LLC, reported 2019-06-12, distributed nationwide. The MX40 may experience increased power consumption and may have a lack of visual and/or audible notifications
| Recall number | Z-1695-2019 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Ongoing |
| Voluntary or mandated | Voluntary |
| Recalling firm | Philips North America, LLC, Andover, MA, United States |
| Recall initiated | 2019-03-28 |
| Classified | 2019-05-31 |
| Reported by FDA | 2019-06-12 |
| Distributed | Nationwide (US) |
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 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 for recall
The MX40 may experience increased power consumption and may have a lack of visual and/or audible notifications while in a Low Battery State .
Machine access
This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/Z-1695-2019. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.
Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.