FDA Class I Recall: Brainlab Cranial Image-Guided Surgery System
The Food and Drug Administration (FDA) has issued a Class I Recall of all Brainlab Cranial Image-Guided Surgery Systems before version 3.0. This comes after findings exposed errors in the navigation system that can lead to serious injury and/or death. The potential for errors in navigation system display in comparison to a patient’s anatomy can lead… Continue reading
