Quick Facts at a Glance
- Recall Date
- October 31, 2025
- Hazard Level
- HIGH
- Brand
- Philips
- Category
- Health & Personal Care
- Sold At
- Unknown
- Geographic Scope
- 1 states
- At-Risk Groups
- GENERAL
What to Do Now
Use this page like a recall checklist: verify the product first, then act on the official remedy.
Immediate steps
- 1Stop using the product until you confirm whether it is included in the recall.
- 2Compare the product label, model number, UPC, color, size, and purchase location against the identifiers below.
- 3Follow the official remedy from FDA - Medical Devices; save photos, receipts, labels, and correspondence before contacting the company.
- 4If the product could harm a child, older adult, pet, or patient, move it out of reach immediately.
Check these identifiers
- Brand
- Philips
- Product type
- Patient Monitor
- Model numbers
- M8102A, 00884838000278
- Sold at
- Unknown
- Where affected
- ALL
Recall Timeline
Key dates and source checks for this recall record.
Recall announced
October 31, 2025
Reported by FDA DEVICE
December 10, 2025
RecallRadar source check
April 18, 2026
Consumer action
Use the official remedy and keep documentation.
Hazard Information
Potential issue where the IntelliVue monitors did not alarm.
What You Should Do
Patients and healthcare providers should stop using this device immediately. Follow the recall instructions provided by the manufacturer. Contact Philips North America Llc or your healthcare provider for instructions. Notification method: Letter
About This Product
The IntelliVue MP2 is a patient monitor used in hospital settings to track vital signs and alert clinicians to changes in patient status.
Why This Is Dangerous
If the monitor fails to alarm, clinicians may miss critical events, delaying intervention and potentially compromising patient safety.
Industry Context
This recall is not part of a broader industry pattern.
Real-World Impact
Hospitals may need to replace or repair affected monitors, adjust monitoring protocols, and implement temporary solutions to ensure patient safety.
Practical Guidance
How to identify if yours is affected
- Confirm model number M8102A on the device label
- Check UDI-DI 00884838000278 on the label
- Note that all serial numbers are included in the recall
Where to find product info
Examine the device label and packaging for model, UDI-DI, and serial number information
What timeline to expect
Replacement or remediation timelines typically 4-8 weeks, depending on hospital procurement and Philips processes
If the manufacturer is unresponsive
- Escalate to hospital procurement and risk management
- Contact Philips recall support through official channels
- File a report with hospital incident logging systems if alarms were missed
How to prevent similar issues
- Regularly review recall notices for critical devices
- During monitoring shifts, periodically test alarm functions
- Establish alternative monitoring capabilities during remediation
Documentation advice
Document recall notice, device identifiers (model, UDI-DI, serial numbers), and communications with Philips for records
Get instant alerts for Health & Personal Care recalls
Be the first to know. Free instant alerts to your inbox.
Product Details
Model numbers: M8102A. UDI-DI: 00884838000278. All Serial Numbers affected. Sold to healthcare facilities worldwide, including US nationwide. When sold: Unknown. Price: Unknown.
Reported Incidents
No injuries or incidents have been reported.
Key Facts
- Quantity recalled: 1,913,441 units
- Model: M8102A
- All serial numbers affected
- Worldwide distribution to healthcare facilities
Browse More Recalls
Safety Guide
Not sure what to do next? Our guide walks you through the process step by step.
Read: What to Do When You Find a Recalled ProductGet Alerts for Health & Personal Care Recalls
Get instant alerts for recalls that affect you. Free forever.