Surgical FDA Alerts

GE Healthcare Recalls Carestation 600 Series Anesthesia Systems Due to Loss of Mechanical Ventilation

Call 1 Recall: Arkon Anesthesia Delivery System recalled due to unexpected failed state while in use or idle

Class 1 Recall: Updated Status of FUJIFILM Medical Systems, U.S.A., Inc. Model ED-530XT Duodenoscopes: FDA Safety Communication

Class 1 Recall: Navigational Accuracy Errors Associated with Frameless Stereotaxic Navigation Systems: FDA Safety Communication

Class 1 Recall: FDA Recommends Health Care Facilities Transition from Custom Ultrasonics Endoscope Washer/Disinfectors to Alternate Reprocessing Methods: FDA Safety Communication

Class 1 Recall: Brainlab Cranial Image-Guided Surgery (IGS) System – Navigation Inaccuracy

Class 1 Recall: FUJIFILM Medical Systems, U.S.A., Inc. Validates Revised Reprocessing Instructions for Model ED-530XT Duodenoscopes: FDA Safety Communication

FDA Recommends Health Care Facilities Transition from Custom Ultrasonics Endoscope Washer/Disinfectors to Alternate Reprocessing Methods: FDA Safety Communication

Class 1 Recall: Supplemental Measures to Enhance Duodenoscope Reprocessing: FDA Safety Communication