Home / Recalls / Medical Devices
QUANTUM SURGICAL SAS recalls The EPIONE device v1.0.2 is a user controlled, stereotactic accessory device intended to assist in the planning and manu
Recalled October 16, 2024 · FDA recall Z-0037-2025 · QUANTUM SURGICAL SAS
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. · FDA Class II
Units
2 units
Sold at
US Nationwide distribution in the state of FL.
Description
Quantum Surgical has become aware that a component (central axis) inside the Needle Guide product (product number 02-0027) is the subject of rust.
Product
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 phase, the desired instrument placement and performance is defined relative to the target anatomy. During the guidance phase, the device enables to monitor respiratory levels and verify patient position prior to instrument advancement. During the assessment phase, the achieved instrument placement and performance are displayed relative to the previously defined plan through an overlay of the pre- and post-treatment image data.
Manufacturer(s)
QUANTUM SURGICAL SAS
Made in
France
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →