Class I Recall of Brainlab AG Spine and Trauma 3D Navigation Software
Brainlab is recalling the Spine & Trauma 3D Navigation Software due to the potential for incorrect information to display during surgery that may prevent the surgeon from accurately navigating surgical tools inside the patient. This may result in:
- Damage to the patient’s body
- A second, otherwise unnecessary, surgical procedure, or
- Serious life-threatening patient injuries or death
Recalled Product Details:
- Brainlab Spine & Trauma 3D Navigation 1.0
- Product code: HAW
- Manufacturing Dates: May 2018 to February 2019
- Distribution Dates: May 2018 to February 2019
- Devices Recalled in the U.S.: 60
Brainlab notified consignees of the problem on March 1, 2019, and directed consignees to:
- Avoid workflow changes with already registered datasets, if possible. For intraoperative screw planning, avoid switching between the workflow application selections “3D Navigation Intraoperative Imaging” and “3D Navigation” during one patient treatment.
- After restarting the application with a previously registered dataset (crash restore or workflow change), always activate and deactivate the sub-menu “Orientation” once to ensure that the correct, expected view representations are displayed for the current session.
- Continue to follow instructions and warnings in the user guide, particularly regarding maintaining navigation accuracy and avoiding reference displacement.
Brainlab plans to stop distributing this software as soon as an updated version is released and available for distribution. For more information, please reference the Navigational Accuracy Errors Associated with Frameless Stereotaxic (Stereotactic) Navigation Systems: FDA Safety Communication, which includes recommendations for health care providers.
The FDA has identified this as a Class I recall, the most serious type of recall. Use of these devices may cause serious injuries or death.
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