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Mazor Robotics Recalls
5 recalls on record · December 26, 2018 to January 28, 2026 · Medical Devices
Recalls by year
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23
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26
Count of recall notices naming this brand, by the year the recall was announced. A quiet year is not proof of a safe year.
January 28, 2026Medical DevicesFDA
Mazor Robotics Ltd recalls Mazor X robotic guidance system REF: TPL0059
Hazard: Software errors that can result in incorrect surgical instrument positioning during spinal surgery.
September 25, 2024Medical DevicesFDA
Mazor Robotics Ltd recalls Mazor X. Model Number REF TPL0059; stereotaxic orthopedic instrument
Hazard: Software anomalies which can result in two separate issues: A lagging screen display during a navigated procedure; or the potential for a mismatch between the navigated screw and the screw information presented on the screen.
October 18, 2023Medical DevicesFDA
Mazor Robotics Ltd recalls MAZOR X robotic guidance system, Model TPL0059, with software versions 4.2.2 or 5.0.1
Hazard: Software update
January 1, 2020Medical DevicesFDA
Mazor Robotics Ltd recalls Snapshot Tracker Kit, Mas2659-01, KIT0898, Rx Only, Non Sterile, UDI: 07290109181868
Hazard: The firm has become aware that the Snapshot Trackers were not manufactured in accordance with specifications and could potentially lead to navigational inaccuracies, which may result in patient injury, e.g. nerve damage or neurological deficit/dysfunction
December 26, 2018Medical DevicesFDA
Mazor Robotics Ltd recalls Carousel MAS1025-01, part of the Brain Surgical Accessories Intra-operative Kit (KIT0295), accessory used with the Renai
Hazard: In some situations the carousel position pin (locker) may cause the carousel upper plate to pop out and the carousel may then inadvertently move.