FDA recall record

Medos International Sarl Velys Enabling Tech Robotic-Assist Station REF: 451611001 recall — FDA Z-3088-2026

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

Class IIclassification
Z-3088-2026official record ID
Sep 9, 2026report date

Recall record at a glance

Official recordZ-3088-2026
CategoryMedical Device Recalls
ClassificationClass II
FDA record statusOngoing
Recalling firmMedos International Sarl
Report dateSep 9, 2026
Recall initiation dateJul 23, 2026
Quantity29 stations
LocationLe Locle, N/A, Switzerland

Official product description

Velys Enabling Tech Robotic-Assist Station REF: 451611001

Why the product was recalled

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

Distribution information

US Nationwide distribution in the states of DE, FL, IL, KY, MD, MI, MN, NJ, NM, NY, OR, PA, TN, TX, VA, WA.

How to read the classification

FDA Class II indicates a situation in which use of or exposure to the product may cause temporary or medically reversible adverse health consequences, or where the probability of serious consequences is remote. The classification shown here comes from the FDA record.

Additional record details

Recall type: Voluntary: Firm initiated. Initial notification: Visit.

What to do next

If you believe you have the recalled product, use the recall number and firm information above to confirm the official notice and follow the instructions issued by the FDA, recalling firm, retailer or product manufacturer. For drugs and medical devices, decisions about treatment or medical care should be discussed with a qualified health professional.

About this record

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