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Philips Medical Systems Nederland B.V. recalls IntelliSpace Cardiovascular, Software 8.0.0.4.
Recalled September 17, 2025 · FDA recall Z-2543-2025 · Philips Medical Systems Nederland B.V
Hazard
Software issue that results in the display of outdated information. · FDA Class II
Units
4 units
Sold at
US Nationwide distribution in the states of GA, NC & TX.
Description
Software issue that results in the display of outdated information.
Product
IntelliSpace Cardiovascular, Software 8.0.0.4.
Manufacturer(s)
Philips Medical Systems Nederland B.V.
Made in
Netherlands
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →