Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
EarlyVue VS30 Vital Signs Monitor Recalled by Philips North America Llc Due to A software issue prevents the monitor from alarming...
What You Should Do
Stop using this product immediately. Do not consume, use, or distribute it.
Return the product to the place of purchase for a full refund. If you have questions, contact Philips North America Llc directly.
Affected Products
EarlyVue VS30 Vital Signs Monitor, utilizing E01 (Oridion Microstream sidestream etCO2) and R21 (Masimo Rainbow RRa) simultaneously, Product Code 863359
Quantity: 13 total devices
Why Was This Recalled?
A software issue prevents the monitor from alarming when the high/low acoustic respiration rate (RRa) limits are violated.
Where Was This Sold?
This product was distributed nationwide across all 50 states.
About Philips North America Llc
Philips North America Llc has 301 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report