FDA Enforcement Class II Ongoing

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.

Recall: Z-1927-2025 · Reported June 18, 2025

Enforcement

Recall Number
Z-1927-2025
Event ID
96967
Classification
Class II
Status
Ongoing
Product Type
Devices
Firm
QUANTUM SURGICAL SAS
Voluntary / Mandated
Voluntary: Firm initiated
Initial Notification
Letter
Report Date
June 18, 2025
Initiation Date
May 23, 2025
Classification Date
June 9, 2025
Address
1000 rue du mas de verchant, ZAC Eureka, montpellier, N/A, France

Description

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

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

Code Info

Model Number: 30-0001 UDI-DI code: 03760305400031 Software Version: 1.0.6.1 Serial Numbers (U.S.): 0322002, 0323006, 0323003 and 0324001

Distribution

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

Quantity

4 units in U.S.