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FDA Clears Olympus Duodenoscope With Design Modifications Intended to Reduce Infection Risk

Wednesday, January 20, 2016   (0 Comments)

The Food and Drug Administration (FDA) announces it has cleared the Olympus TJF-Q180V duodenoscope with modifications to the device’s design and labeling intended to help reduce the risk of bacterial infections. Olympus will voluntarily recall its original model currently being used in healthcare facilities and make the needed repair as quickly as possible.


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