Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
EarlyVue VS30 Vitals monitor with Software Versions A.00.02 and A.00.01 Recalled by Philips North America Llc Due to EarlyVue VS30 Vital Signs Monitor and EarlyVue VS30...
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 Vitals monitor with Software Versions A.00.02 and A.00.01 Product Number: 863380
Quantity: 1421 units US; 3 units OUS
Why Was This Recalled?
EarlyVue VS30 Vital Signs Monitor and EarlyVue VS30 Vitals monitor Missing Calibration Alarm, a risk of an inaccurate CO2 measurement which may lead to a failure to recognize a change in patient condition.
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