Class II
Medical Device Recall: Velys Enabling Tech Robotic-Assist Station REF: 451611001
Medos International Sarl · July 23, 2026
Reason for Recall
Software issue within robotic controller which may cause unintended movement of the robotic arm during bone preparation or instrument positioning.
Distribution
US Nationwide distribution in the states of DE, FL, IL, KY, MD, MI, MN, NJ, NM, NY, OR, PA, TN, TX, VA, WA.
States Affected
NATIONWIDE
Quantity Affected
29 stations
Source: FDA (openFDA Device Enforcement)
Recall number: Z-3088-2026
Status: ongoing
SafeCheck provides drug interaction information from FDA-approved product labeling (openFDA). This is for informational purposes only and is not medical advice. Always consult your healthcare provider before making medication decisions.