FDAFebruary 27, 2019device

Spine & Trauma 3D Navigation 1.0 (subpart of the system Navigation Software Spine & Trauma 3D, Version 3.0 ) Intended Use The Spine & Trauma Navigation System is intended as an intraoperative image-guided localization system to enable minimally invasive surgery.

Official recall recorded by the U.S. Food & Drug Administration.

The hazard

In certain occurrences, the affected navigation software application might unexpectedly display a navigated instrument in an axial, coronal/sagittal (ACS) view representation with fixed planes in the image reconstruction (the not-updated ACS view ), instead of displaying the desirable view representation Inline View , which is commonly used for navigating invasive instruments at the spine. This could lead the surgeon to be unable to determine the position of the navigated instrument. This might occur after a crash restore or after changing between different navigation workflows during the same patient treatment.

What to do

FDA enforcement status: Terminated

Brands named

brainlab agbrainlab

UPCs

04056481140328

Recall history

Other federal recalls tied to the same brand — a factual pattern, straight from the source data.

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