FDA recall Z-0037-2025

QUANTUM SURGICAL SAS · Class II · device

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.

Reason for recall

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

Distribution

US Nationwide distribution in the state of FL.

Key facts

Status
Completed
Initiation date
2024-08-05
Report date
2024-10-16
Voluntary/Mandated
Voluntary: Firm initiated
Location
montpellier, France

Primary source

https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-0037-2025