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FDASeptember 12, 2025device

Cardiac Workstation 7000; Model Number: 860441;

Official recall recorded by the U.S. Food & Drug Administration.

The hazard

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

What to do

FDA enforcement status: Ongoing

Brands named

philips north americaphilipsphilips north

UPCs

00884838094833

Recall history

Other federal recalls tied to the same brand — a factual pattern, straight from the source data.

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