FDAMarch 29, 2022device

The device is a whole-body CT x-ray system. The acquired x-ray transmission data is reconstructed by computer into cross-sectional images of the body taken at different angles and planes. The system also includes signal analysis and display equipment, patient and equipment supports, components, a...

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

The hazard

Three software issues affecting incorrect image display, error interpreting patient images due to image reporting, and patient exposure to incorrect image/function during clinical use.

What to do

FDA enforcement status: Completed

Brands named

philips north americaphilipsphilips north

UPCs

0088483810550800884838085015

Recall history

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

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