QUANTUM SURGICAL SAS: Medical Device Recall in 2024 - (Recall #: Z-0037-2025)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2024.

Data Source: FDA.
Product Description:

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.

Product Classification:

Class II

Date Initiated: August 5, 2024
Date Posted: October 16, 2024
Recall Number: Z-0037-2025
Event ID: 95194
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.

Status: Completed
Product Quantity: 2 units
Code Information:

UDI/DI 37603054002NGXL, serial numbers: 0321015 and 0321017

Distribution Pattern:

US Nationwide distribution in the state of FL.

Voluntary or Mandated:

Voluntary: Firm initiated