FDA Issues Class I Recall for Contaminated Spinal Anesthesia Kits

B. Braun Medical, Inc. has initiated a Class I recall, the most serious type, for specific spinal anesthesia kits. The recall is due to the presence of contaminated bupivacaine, posing risks of infection, inflammation, and reduced effectiveness. There is particular concern for potential cerebral fluid contamination and meningitis when used in the neuraxial space.