FDA recall record

Philips Cardiac Workstation 7000 recall — FDA Z-2956-2026

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

Class IIclassification
Z-2956-2026official record ID
Aug 26, 2026report date

Recall record at a glance

Official recordZ-2956-2026
CategoryMedical Device Recalls
ClassificationClass II
FDA record statusOngoing
Recalling firmPhilips North America LLC
Report dateAug 26, 2026
Recall initiation dateJul 1, 2026
Quantity1,810 units
LocationCambridge, MA, United States

Official product description

Cardiac Workstation 7000. Product Number: 860441.

Why the product was recalled

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

Distribution information

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.

How to read the classification

FDA Class II indicates a situation in which use of or exposure to the product may cause temporary or medically reversible adverse health consequences, or where the probability of serious consequences is remote. The classification shown here comes from the FDA record.

Additional record details

Recall type: Voluntary: Firm initiated. Initial notification: Letter.

What to do next

If you believe you have the recalled product, use the recall number and firm information above to confirm the official notice and follow the instructions issued by the FDA, recalling firm, retailer or product manufacturer. For drugs and medical devices, decisions about treatment or medical care should be discussed with a qualified health professional.

About this record

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