Medical DeviceJan 28, 2026
Mazor X robotic guidance system REF: TPL0059 recall — FDA Z-1122-2026
Software errors that can result in incorrect surgical instrument positioning during spinal surgery.
Class IIFDA: OngoingMazor Robotics Ltd
Recall history in this database
Classification mix: Class II: 4.
Medical DeviceSep 25, 2024
Mazor X. Model Number REF TPL0059; stereotaxic orthopedic instrument recall — FDA Z-3156-2024
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…
Class IIFDA: OngoingMazor Robotics Ltd
Medical DeviceJan 1, 2020
Mazor Robotics Snapshot Tracker Kit, Mas2659-01, KIT0898, Rx Only, Non Sterile, UDI recall — FDA Z-0721-2020
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…
Class IIFDA: TerminatedMazor Robotics Ltd
Medical DeviceDec 26, 2018
Mazor Robotics Carousel MAS1025-01, part of the Brain Surgical Accessories Intra-operative recall — FDA Z-0609-2019
In some situations the carousel position pin (locker) may cause the carousel upper plate to pop out and the carousel may then inadvertently move.
Class IIFDA: TerminatedMazor Robotics Ltd
Understanding this recall history
This page summarizes recall records in which the official source identifies Mazor Robotics Ltd as the recalling firm or manufacturer. The number of records should not be treated as a safety rating or a measure of company size, because recall counts depend on product mix, reporting periods and how government records are organized.
Compare the dates, categories and classifications together rather than relying on the total alone. Open an individual record for the recalled product, reason, distribution details and current instructions available from the source.