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Philips North America recalls Cardiac Workstation 7000; Model Number: 860441;
Recalled October 22, 2025 · FDA recall Z-0166-2026 · Philips North America
Hazard
Failure of Environmental Stress Testing from a pinched power module wire within the housing of the Cardiac Workstation device which resulted in a short. · FDA Class II
Units
29 units
Sold at
US Nationwide distribution in the states of CA, IA, TN, TX, VA.
Description
Failure of Environmental Stress Testing from a pinched power module wire within the housing of the Cardiac Workstation device which resulted in a short.
Product
Cardiac Workstation 7000; Model Number: 860441;
Manufacturer(s)
Philips North America
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →