Duodenoscopes FDA Alerts

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

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

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