FDAJuly 14, 2025device

3mensio Workstation (Vascular Fenestrated) software

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

The hazard

When fenestrated analysis with clock measurements is started in diagnostic bioimaging software (intended to measure/visualize cardiovascular structures) and the 12h position of a single clock is changed, other clock measurements are not updated relative to the new 12h position which may cause stent graft fenestrations at incorrect position, which may lead to blood flow disruption and tissue damage

What to do

FDA enforcement status: Ongoing

Brands named

pie medical imaging b vpiepie medical

UPCs

0805630445550508056304455925

Recall history

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

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