FDAMay 23, 2025device

EPIONE Model 30-0001 UDI-DI code: 03760305400031 The EPIONE¿ device is a user controlled, stereotactic accessory intended to assist in the planning and manual advancement of one or more instruments, as well as in verification of instrument position during Computed Tomography (CT) guided percutane...

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

The hazard

Due to a software bug the robotic arm may incorrectly guide the instrument compared to the planning defined by user.

What to do

FDA enforcement status: Ongoing

Brands named

quantum surgical sasquantumquantum surgical

UPCs

03760305400031

Recall history

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

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