FDAMay 29, 2025device

Spectral CT. Computed tomography X-ray system.

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

The hazard

Devices with affected software may experience two unintended motion issues that may lead to contact between the Gantry or table with the operator or patient, along with additional software issues that affect CT performance.

What to do

FDA enforcement status: Ongoing

Brands named

philips north americaphilipsphilips north

UPCs

00884838101111

Recall history

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

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