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Recall database

Orthopedic Augmented Reality recalls

Drawn from openFDA device enforcement reports. Filter by severity, status, state, year, or manufacturer.

Showing 1–2 of 2 recalls

Class IIOngoingZ-2957-2026

Kico Knee Innovation Company recalls Brand Name: Kico Knee Innovation Product Name: ARVIS SURGICAL NAVIGATION SYSTEM GEN 2…

Due to an internal sensor issue, image displayed with eyepiece may appear tilted relative to the eyepiece housing

Kico Knee Innovation C…Aug 26, 2026

Class IIOngoingZ-0145-2026

Kico Knee Innovation Company recalls Brand Name: ARVIS Product Name: ARVIS" Shoulder Model/Catalog Number: IN-27300

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

Kico Knee Innovation C…Oct 22, 2025