Olympus Corporation of the Americas: Medical Device Recalls in 2017

According to to data from the FDA, there were 4 medical device recalls made by Olympus Corporation of the Americas in 2017. See the details of the recalls below.

You can see similar recalls for other firms.

• Olympus ENDOEYE HD II Video Telescopes Models: WA50040A Endoeye HD II, 10 mm, 0 deg., autoclavable; WA50042A Endoeye HD II, 10 mm, 30 deg., autoclavable; repair cable 10mm 0/30 deg., part number W7100603
• Uretero-reno videoscope URF-V2 and URF-V2R endoscope and accessories The URF-V2/V2R endoscopes are intended for use in endoscopic diagnosis and treatment within the ureter and kidney.
• High Frequency Resection Electrodes, endoscope, ac-powered and accessories The electrodes are used for endoscopic diagnosis and treatment in urological and gynecological applications.
• URF-P6 Uretero-reno fiberscope and URF-P6R Uretero-reno fiberscope