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FDAFebruary 24, 2021device

Philips CT systems are advanced continuous-rotation computed tomography systems suitable for a wide range of computed tomographic (CT) applications - Product Usage: intended for use in the head and whole body.

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

The hazard

Philips has internally detected an issue with the actuators used in the Incisive CT couch, which could result in the couch failure to self-lock, and unexpectedly moving slowly downward to its limit position.

What to do

FDA enforcement status: Terminated

Brands named

philips healthcare suzhouphilipsphilips healthcare

UPCs

0088483805984900884838085015

Recall history

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

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