Philips recalls IntelliVue MP5 monitors (product number M810:5A) due to potential failure to alarm. Affected units may not alert users to critical health changes.
Potential issue where the IntelliVue monitors did not alarm.
Philips is recalling IntelliVue MP5 monitors that may not alarm properly. This could mean critical health changes go unnoticed, risking serious injury or death.
The monitors may fail to sound alarms when critical health changes occur. This could delay life-saving interventions if a patient's condition worsens without warning.
Patients using these monitors at home or in hospitals are most at risk. Healthcare providers and caregivers who rely on the device for monitoring are also affected.
Check for product number M8105A on the monitor. Units sold with serial numbers starting with 'All' are affected. The UDI-DI code 00884838000230 is also associated with this recall.
Look for product number M8105A on the monitor's label.
Reach out to Philips customer service for further instructions on the recall.
The monitors may not alarm properly, which could delay critical health interventions.
Check for product number M8105A on the monitor or serial numbers starting with 'All'.
Contact Philips customer service for instructions on the recall.
We’ve drafted a message you can send Philips to request your refund or repair — edit it as you like.
Subject: Recall Z-0850-2026 — Philips Philips Hello, I own a Philips that is covered by recall Z-0850-2026 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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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.
