FDA recall Z-1927-2025

QUANTUM SURGICAL SAS · Class II · device

Product

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 percutaneous ablation procedures in the abdomen, performed by physicians trained for CT procedures and performed under general anaesthesia with rigid straight instruments such as needles and probes of diameters ranging from 11G to 19G.

Reason for recall

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

Distribution

Worldwide distribution - U.S. Nationwide distribution in the states of FL,IL, IN, and TX. The countries of France, Germany and United Kingdom.

Key facts

Status
Ongoing
Initiation date
2025-05-23
Report date
2025-06-18
Voluntary/Mandated
Voluntary: Firm initiated
Location
montpellier, France

Primary source

https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-1927-2025