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FDA · Medical devices ·

Cardiac Workstation 7000 recall

Philips North America Llc recalled Cardiac Workstation 7000 on August 26, 2026 because of device will intermittently provide inaccurate data related to native heart rate. It was sold nationwide.

Why it was recalled

Device will intermittently provide inaccurate data related to native heart rate.

What's recalled

Cardiac Workstation 7000. Product Number: 860441.

Quantity: 1,810 units

What to do

Check whether you have the product (match the lot numbers, dates or codes in the official notice). Stop using it, and return it or throw it away as the notice says.

Read the official FDA notice

Details

Company
Philips North America Llc, Cambridge, MA
Date
Severity
Class II
the product could cause temporary or reversible health problems.
Where sold
Nationwide
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, Po…
Status
Ongoing
Recall number
Z-2956-2026
Source
U.S. Food and Drug Administration

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