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Philips North America Llc recalls Cardiac Workstation 5000. Product Number: 860439.
Recalled August 26, 2026 · FDA recall Z-2955-2026 · Philips North America
Hazard
Device will intermittently provide inaccurate data related to native heart rate. · FDA Class II
Units
796 units
Sold at
Worldwide distribution - US Nationwide and the countries of Australia, Austria, Bahrain, Belgium, Brazil, Canada, Croatia, Czech Republic, Dominican Republic, France, Germany, Gibraltar, Hong Kong, Iceland, Ireland, Iraq, Italy, Luxembourg, Malta, Netherlands, New Caledonia, New Zealand, Norway, Poland, Portugal, Qatar, Saudi Arabia, Serbia, Singapore, Slovakia, Slovenia, South Korea, Spain, Sweden, Switzerland, Taiwan, Thailand, United Arab Emirates, United Kingdom.
Description
Device will intermittently provide inaccurate data related to native heart rate.
Product
Cardiac Workstation 5000. Product Number: 860439.
Manufacturer(s)
Philips North America Llc
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →