PlainRecalls
FDA Devices Moderate Class II Ongoing

Cardiac Workstation 5000; Model Number: 860439;

Reported: October 22, 2025 Initiated: September 12, 2025 #Z-0165-2026

Product Description

Cardiac Workstation 5000; Model Number: 860439;

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.

Details

Recalling Firm
Philips North America
Units Affected
28 units
Distribution
US Nationwide distribution in the states of CA, IA, TN, TX, VA.
Location
Cambridge, MA

Frequently Asked Questions

What product was recalled?
Cardiac Workstation 5000; Model Number: 860439;. Recalled by Philips North America. Units affected: 28 units.
Why was this product recalled?
Failure of Environmental Stress Testing from a pinched power module wire within the housing of the Cardiac Workstation device which resulted in a short.
Which agency issued this recall?
This recall was issued by the FDA Devices on October 22, 2025. Severity: Moderate. Recall number: Z-0165-2026.