FDANovember 12, 2021device

ACUSON Sequoia Ultrasound Imaging System with Software Version VA25A/B

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

The hazard

Due to a calculation error in the measurement when using 2D trace (manual trace) tool. The trace circumference value is overestimated and may potentially result in misdiagnosis of a patient's condition.

What to do

FDA enforcement status: Ongoing

Brands named

siemens medical solutionssiemenssiemens medical

Recall history

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

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