FDADecember 24, 2020device

PHILIPS Incisive Computed tomography X-ray system Incisive CT Software Upgrade from V4.5.1.41921 to V4.5.1.41989-Intended to produce cross-sectional images of the body Model Number: 728143

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

The hazard

Patient tabletop moved out to the home position during scan initialization, may cause operator/bystander staying by the rear of the table to collide with the moved tabletop and be injured

What to do

FDA enforcement status: Ongoing

Brands named

philips north americaphilipsphilips north

UPCs

00884838085015

Recall history

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

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