Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
Philips IntelliSpace Cardiovascular software Recalled by Philips Medical Systems Nederland B.V. Due to Study data is not able to be archived,...
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
Philips IntelliSpace Cardiovascular software, Model 830089.
Quantity: 139
Why Was This Recalled?
Study data is not able to be archived, copied, or exported with the cardiovascular software version.
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