Olympus Corporation of the Americas: Medical Device Recalls in 2016

According to to data from the FDA, there were 4 medical device recalls made by Olympus Corporation of the Americas in 2016. See the details of the recalls below.

You can see similar recalls for other firms.

• Olympus TJF-Q180V flexible gastrointestinal Duodenoscope Product Usage: This instrument has been designed to be used with an Olympus video system center, light source, documentation equipment, monitors, EndoTherapy accessories, and other ancillary equipment for endoscopy and endoscopic surgery within the duodenum.
• HF Cable WA00014A, Endoscopic electrosurgical unit and accessories
• OER-Pro Endoscope Reprocessor, Endoscope washer/disinfector
• EVIS EXERA Duodenovideoscope Olympus TJF Type 160F/VF used with an Olympus video system center, light source, documentation equipment monitors, Endo Therapy accessories and other ancillary equipment for endoscopy and endoscopic surgery within the duodenum.