FDAMay 1, 2021device

Continuous CT Fluoroscopy DVI Ceiling Mount CCT Arm DVI Option - Monitor 728332 - IQon Spectral CT : IQon Spectral CT

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

The hazard

Significant wear of the Monitor Bracket Assembly shaft goes unrecognized could potentially lead to the Monitor Bracket Assembly detaching from the Suspension Arm and result in potential hazard for the monitor to fall while remaining attached to the cables resulting in patient, operator, bystander, or service person to serious injury.

What to do

FDA enforcement status: Ongoing

Brands named

philips north americaphilipsphilips north

UPCs

728332860005728332395001728332860043008848380595427283328601317283328600507283328601227283326003872833286017772833286018572833286017272833260051

Recall history

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

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Continuous CT Fluoroscopy DVI Ceiling Mount CCT Arm DVI Option - Monitor 728332 - IQon Spectral CT : IQon Spectral CT — Recall Details · AllClear