Day

September 9, 2025
09
Sep

FDA Recall: Software issue that results in the display of outdated information.

September 9, 2025
Company: Philips Medical Systems Nederland B.V. Date of Enforcement Report: 9/9/2025 Class: II PRODUCT IntelliSpace Cardiovascular, Software 8.0.0.4. Recall Number: Z-2543-2025 REASON: Software issue that results in the display of outdated information. RECALLING FIRM/MANUFACTURER: Philips Medical Systems Nederland B.V. QUANTITY: 4 units DISTRIBUTION: US Nationwide distribution in the states of GA, NC & TX.
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