Kico Knee Innovation Company: Device Recall

Recall #Z-0145-2026 · 09/19/2025

Class II: Risk

Recall Details

Recall Number: Z-0145-2026
Classification: Class II
Product Type: Device
Recalling Firm: Kico Knee Innovation Company
Status: Ongoing
Date Initiated: 09/19/2025
Location: Pymble, Australia
Voluntary/Mandated: Voluntary: Firm initiated
Product Quantity: 21 systems

Reason for Recall

Complaint identified issue with AI surgical planning software that may result in implant malalignment and/or decrease range of motion.

Product Description

Brand Name: ARVIS Product Name: ARVIS" Shoulder Model/Catalog Number: IN-27300, Arvis Surgical Planning Software Software Version: V2025.1.2 Product Description: Intended Use: The ARVIS" system is a computer-controlled navigation system intended to provide intra-operative measurements to the surgeon to aid in selection and positioning of orthopedic implant components. Description: ARVIS Shoulder is a computer-controlled surgical navigation system for shoulder arthroplasty. It aids the surgeon in making intra-operative measurements and locating anatomical structures of the shoulder joint based on the patient s preoperative imaging to assist with selection and positioning of orthopedic implant components. The system consists of software, electronic hardware and surgical instruments. The device s workflow involves CT based preoperative planning followed by intraoperative navigation and execution. The preoperative planning software enables 3D virtual implant positioning based on the patient s CT reconstructed digital bone model and bony landmarks. The shoulder navigation application software then matches the patient s digital bone model and landmarks to the intraoperative landmarks registered by the surgeon, allowing an image-based navigation to follow. The surgeon uses the plan data as guidance to navigate and help position shoulder instruments and implants.

Distribution Pattern

US Nationwide distribution in the states of IN, MN, MO, OH, FL, IL, RI, KY, CA, WI, MI, PA, WA, CO, AL.

Data from FDA openFDA enforcement reports. This site is not affiliated with or endorsed by the FDA. Recall information may be updated by the FDA at any time.