FDAAugust 5, 2024device

The EPIONE device v1.0.2 is a user controlled, stereotactic accessory device 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 percutaneous procedures. During the planning ...

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

The hazard

Quantum Surgical has become aware that a component (central axis) inside the Needle Guide product (product number 02-0027) is the subject of rust.

What to do

FDA enforcement status: Completed

Brands named

quantum surgical sasquantumquantum surgical

Recall history

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

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