Class II

Medical Device Recall: Cardiac Workstation 5000; Model Number: 860439;

Philips North America · September 12, 2025

Reason for Recall

Failure of Environmental Stress Testing from a pinched power module wire within the housing of the Cardiac Workstation device which resulted in a short.

Distribution

US Nationwide distribution in the states of CA, IA, TN, TX, VA.

States Affected

NATIONWIDE

Quantity Affected

28 units

Source: FDA (openFDA Device Enforcement)

Recall number: Z-0165-2026

Status: ongoing

SafeCheck provides drug interaction information from FDA-approved product labeling (openFDA). This is for informational purposes only and is not medical advice. Always consult your healthcare provider before making medication decisions.

Philips North America Medical Device Recall: Cardiac Workstation 5000; Model Number: 860439; | SafeCheck