Fresh Recalls

Medos International Sarl recalls

Recall found. Medos International Sarl is named in FDA Class II recall Z-3088-2026 covering Velys Enabling Tech Robotic-Assist Station REF. Hazard: Software issue within robotic controller which may cause unintended movement of the robotic arm during bone preparation or instrument positioning. Identifying details: UDI: 10705034645995/Serial Numbers: W14316295301 W15316297501 W15316298001 W17316322901 W17316323301 W21316347401 W21316347501 W21316347601 W21316347801 W21316347901 W21316348001 W22316365801 W34316479001 W34316479101 W34316479201 W34316479301 W34316479401 W34316479601 W34316479801 W34316480001 W34316480101 W49316554301 W51316597001 W51316597101 Y03316603601 Y03316603701 Y03316603801 Y07316625901 Y15316690901. Status: Ongoing.

Models with recalls

Velys Enabling Tech Robotic-Assist Station REF (1)

All Medos International Sarl recalls

FDA Class II · Medical device · September 9, 2026

Velys Enabling Tech Robotic-Assist Station REF recall — Medos International Sarl

Software issue within robotic controller which may cause unintended movement of the robotic arm during bone preparation or instrument positioning.

Official ID Z-3088-2026 · Official record ↗

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Compiled from official public-domain government data. Last checked October 22, 2026 at 6:00 PM UTC.