FDAAugust 2, 2023device

Incisive CT, software version 5.0

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

The hazard

Philips has identified three software issues with compliance concerns to Subchapter J: Issue 1: Coronary Computed Tomography Angiography (CTA) scan may not be triggered at the optimal time. Issue 2: Use of aborted surview for scan planning will result in deviation from intended scan area. Issue 3: Actual clinical scan with bariatric (Noah) couch will deviate from the intended scan area if surview scan length is greater than 1832mm.

What to do

FDA enforcement status: Ongoing

Brands named

philips healthcarephilips

Recall history

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

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