FDAApril 1, 2025device

Philips Brilliance CT Big Bore, Software Version 4.8.0.10430. Computed Tomography X-Ray System.

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

The hazard

Unintended motion issues related to Interventional Control that may lead to collision of the Gantry/table with the operator or patient.

What to do

FDA enforcement status: Ongoing

Brands named

philips north americaphilipsphilips north

UPCs

00884838098725008848380594500084522500303600884838095168008452250030500088483810114200845225003043

Recall history

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

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