Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
IntelliSpace Cardiovascular Recalled by Philips Medical Systems Nederland B.V. Due to Software issue that results in the display of...
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 Medical Systems Nederland B.V. directly.
Affected Products
IntelliSpace Cardiovascular, Software 8.0.0.4.
Quantity: 4 units
Why Was This Recalled?
Software issue that results in the display of outdated information.
Where Was This Sold?
This product was distributed nationwide across all 50 states.
About Philips Medical Systems Nederland B.V.
Philips Medical Systems Nederland B.V. has 8 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report