Philips IntelliVue MX100 Patient Monitor Recall: No Alarms May Cause Missed Alerts

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Contact the company & request your remedy

Recalling firmPhilips North America Llc222 Jacobs St · Cambridge, MA 02141-2289

No email on file — write to the address above instead.

✎ GovInfoNow plain-language explainer

What happened, in plain English

Philips is recalling IntelliVue MX100 patient monitors because they may not sound alarms during critical events. This could lead to missed medical alerts and potential harm to patients.

Why it’s dangerous

The monitors may not sound alarms when needed, which could cause critical medical events to go unnoticed. This risk is highest in hospital settings where timely alerts are essential for patient safety.

Who’s affected

Healthcare providers using the IntelliVue MX100 patient monitors are most at risk. Patients in hospitals or clinics with this monitor could be affected if alarms fail.

How to tell if you have this one

Check for the product number 867033 on the monitor. All units were sold with this model and serial numbers.

Brand
Philips
Category
Medical device

Based on the official FDA remedy

What to do — step by step

Check Monitor Serial Number
Look for the product number 867033 on the monitor's label to confirm if it's affected.

✎ GovInfoNow

Questions people ask

Why is this monitor being recalled?

The IntelliVue MX100 patient monitors may not alarm during critical events, which could lead to missed medical alerts.

How can I tell if my monitor is affected?

Check for the product number 867033 on the monitor's label. All units with this model number are affected.

What should I do if I have this monitor?

Contact Philips directly to confirm if your monitor is affected and get instructions for next steps.

Take action

Contact Philips

We’ve drafted a message you can send Philips to request your refund or repair — edit it as you like.

✉️ Open in email

Subject: Recall Z-0861-2026 — Philips Philips

Hello,

I own a Philips that is covered by recall Z-0861-2026 from Philips.

I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this?

Thank you.

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Where this comes from

The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.

Official source: FDA Recall #Z-0861-2026 (October 31, 2025) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for Z-0861-2026 to see it in context.
Plain-language summary written by qwen3:4b on August 10, 2026, from the official record above. Not reviewed by a person — if it conflicts with the FDA notice, the notice is correct. Report an error on this page.
GovInfoNow is an independent service and is not a government agency. We republish official FDA recall data; we don’t issue, amend or administer recalls.

Philips North America Llc recalls IntelliVue Patient Monitor MX100. Product Number: 867033.

Use caution until it’s fixed