Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
Philips SureSigns VSi/VS2+ patient monitors Model Part Numbers VSi/ 863275 Recalled by Philips Healthcare Inc. Due to Philips SureSigns VSi/VS2+ patient monitors may not be...
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 Healthcare Inc. directly.
Affected Products
Philips SureSigns VSi/VS2+ patient monitors Model Part Numbers VSi/ 863275, 863276, 863277, VS2+ 863278, 863279. The SureSigns VS2+ vital signs monitor is for monitoring, recording and alarming of multiple physiological parameters of adults, pediatrics, and neonates in healthcare environments. Additionally, the monitor is intended for use in transport situations within a healthcare facility. The SureSigns VSi vital signs monitor is for measurement of multiple physiological parameters of adults, pediatrics, and neonates in healthcare environments. Additionally, the monitor is intended for use in transport situations within a healthcare facility
Quantity: 2314 units
Why Was This Recalled?
Philips SureSigns VSi/VS2+ patient monitors may not be properly secured and may fall from the wall mount
Where Was This Sold?
This product was distributed nationwide across all 50 states.
About Philips Healthcare Inc.
Philips Healthcare Inc. has 36 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report