IntelliVue Patient Monitor MX850. Product Number: 866470.
Pending LLM rewrite. Source: FDA_DEVICE Z-0870-2026.
Severity not yet assessed
We have not scored this recall against our rubric yet, so we are not showing a severity rating or our usual guidance. The agency’s own notice below is the authoritative source — read it first.
Plain-English summary
Potential issue where the IntelliVue monitors did not alarm.
The recalled product
- Product
- IntelliVue Patient Monitor MX850. Product Number: 866470.
- Manufacturer
- Philips North America Llc
- Category
- Medical Device — Devices
Is your product affected?
Check your packaging against the codes below. If any of them match, the product is part of this recall.
Lot numbers (3)
- Product Number: 866470
- UDI-DI: 00884838070790
- All Serial No.
Distribution
Distributed nationwide across the United States.
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