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Olympus Corporation of the Americas Recalls
414 recalls on record · October 7, 2015 to July 29, 2026 · Medical Devices
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Count of recall notices naming this brand, by the year the recall was announced. A quiet year is not proof of a safe year.
October 23, 2019Medical DevicesFDA
Olympus Corporation of the Americas recalls Berkeley Disposa-Filter used with Berkeley VC-10 Vacuum Curettage System - Product Usage: designed for rapid transcervic
Hazard: Berkeley Disposa-Filter may possess an insufficient ultrasonic weld defect which joins the two-halves of the filter cartridge, thus the housing could separate
August 14, 2019Medical DevicesFDA
Olympus Corporation of the Americas recalls Olympus MAJ-209 Single Use Suction Valves, Model Number MAJ-209 Product Usage: This product has been designed to be
Hazard: There is a potential for the single use suction valve to come apart and/or remain stuck inside the endoscope.
July 24, 2019Medical DevicesFDA
Olympus Corporation of the Americas recalls Olympus WM-NP2 or WM-DP2 Mobile Workstations with Nurse Control Panel Arm, Model. No. MAJ-1664
Hazard: WM-NP/DP2 workstations could become unstable and may fall over if the control panel arm is mounted with a video monitor weighing more than 19.8 pounds.
March 20, 2019Medical DevicesFDA
Olympus Corporation of the Americas recalls Olympus TJF-Q180V Duodenoscope - Product Usage: These endoscopes are intended for use in endoscopic diagnosis and treatm
Hazard: The adhesive used in the repair of the endoscope was incorrectly prepared. It is unknown what affect the nonconforming adhesive mixture would have on the durability or effectiveness of the gluing operation for the endoscope repair.
March 20, 2019Medical DevicesFDA
Olympus Corporation of the Americas recalls Olympus PCF-Q180AC Video Colonoscope - Product Usage: These endoscopes are intended for use in endoscopic diagnosis and
Hazard: The adhesive used in the repair of the endoscope was incorrectly prepared. It is unknown what affect the nonconforming adhesive mixture would have on the durability or effectiveness of the gluing operation for the endoscope repair.
March 20, 2019Medical DevicesFDA
Olympus Corporation of the Americas recalls Olympus GIF-H180J Gastrointestinal Videoscope - Product Usage: These endoscopes are intended for use in endoscopic diagn
Hazard: The adhesive used in the repair of the endoscope was incorrectly prepared. It is unknown what affect the nonconforming adhesive mixture would have on the durability or effectiveness of the gluing operation for the endoscope repair.
March 20, 2019Medical DevicesFDA
Olympus Corporation of the Americas recalls Olympus GF-UCT180 Ultrasound Gastrovideoscope - Product Usage: These endoscopes are intended for use in endoscopic diagn
Hazard: The adhesive used in the repair of the endoscope was incorrectly prepared. It is unknown what affect the nonconforming adhesive mixture would have on the durability or effectiveness of the gluing operation for the endoscope repair.
October 10, 2018Medical DevicesFDA
Olympus Corporation of the Americas recalls Bronchovideoscope BF-1T40
Hazard: The attachment of non-Olympus accessories to the bronchoscope s instrument channel port may have resulted in more applied force than expected and lead to loosening of the instrument channel port.
October 10, 2018Medical DevicesFDA
Olympus Corporation of the Americas recalls Airway Mobilescope MAF-TM
Hazard: The attachment of non-Olympus accessories to the bronchoscope s instrument channel port may have resulted in more applied force than expected and lead to loosening of the instrument channel port.
October 10, 2018Medical DevicesFDA
Olympus Corporation of the Americas recalls Rhino Laryngo scope ENF-VT2
Hazard: The attachment of non-Olympus accessories to the bronchoscope s instrument channel port may have resulted in more applied force than expected and lead to loosening of the instrument channel port.
October 10, 2018Medical DevicesFDA
Olympus Corporation of the Americas recalls Bronchofiberscope BF-XT40
Hazard: The attachment of non-Olympus accessories to the bronchoscope s instrument channel port may have resulted in more applied force than expected and lead to loosening of the instrument channel port.
October 10, 2018Medical DevicesFDA
Olympus Corporation of the Americas recalls Bronchovideoscope BF-XT160
Hazard: The attachment of non-Olympus accessories to the bronchoscope s instrument channel port may have resulted in more applied force than expected and lead to loosening of the instrument channel port.
October 10, 2018Medical DevicesFDA
Olympus Corporation of the Americas recalls Bronchofiberscope BF-XP60
Hazard: The attachment of non-Olympus accessories to the bronchoscope s instrument channel port may have resulted in more applied force than expected and lead to loosening of the instrument channel port.
October 10, 2018Medical DevicesFDA
Olympus Corporation of the Americas recalls Bronchofiberscope BF-XP40
Hazard: The attachment of non-Olympus accessories to the bronchoscope s instrument channel port may have resulted in more applied force than expected and lead to loosening of the instrument channel port.
October 10, 2018Medical DevicesFDA
Olympus Corporation of the Americas recalls Bronchovideoscope BF-XP160F
Hazard: The attachment of non-Olympus accessories to the bronchoscope s instrument channel port may have resulted in more applied force than expected and lead to loosening of the instrument channel port.
October 10, 2018Medical DevicesFDA
Olympus Corporation of the Americas recalls Ultrasonic Bronchoscope BF-UC180F
Hazard: The attachment of non-Olympus accessories to the bronchoscope s instrument channel port may have resulted in more applied force than expected and lead to loosening of the instrument channel port.
October 10, 2018Medical DevicesFDA
Olympus Corporation of the Americas recalls Ultrasonic Bronchoscope BF-UC160F-OL8
Hazard: The attachment of non-Olympus accessories to the bronchoscope s instrument channel port may have resulted in more applied force than expected and lead to loosening of the instrument channel port.
October 10, 2018Medical DevicesFDA
Olympus Corporation of the Americas recalls Bronchovideoscope BF-Q180-AC
Hazard: The attachment of non-Olympus accessories to the bronchoscope s instrument channel port may have resulted in more applied force than expected and lead to loosening of the instrument channel port.
October 10, 2018Medical DevicesFDA
Olympus Corporation of the Americas recalls Bronchovideoscope BF-Q180
Hazard: The attachment of non-Olympus accessories to the bronchoscope s instrument channel port may have resulted in more applied force than expected and lead to loosening of the instrument channel port.
October 10, 2018Medical DevicesFDA
Olympus Corporation of the Americas recalls Bronchofiberscope BF-P60
Hazard: The attachment of non-Olympus accessories to the bronchoscope s instrument channel port may have resulted in more applied force than expected and lead to loosening of the instrument channel port.
October 10, 2018Medical DevicesFDA
Olympus Corporation of the Americas recalls Bronchofiberscope BF-P40
Hazard: The attachment of non-Olympus accessories to the bronchoscope s instrument channel port may have resulted in more applied force than expected and lead to loosening of the instrument channel port.
October 10, 2018Medical DevicesFDA
Olympus Corporation of the Americas recalls Bronchovideoscope BF-P240
Hazard: The attachment of non-Olympus accessories to the bronchoscope s instrument channel port may have resulted in more applied force than expected and lead to loosening of the instrument channel port.
October 10, 2018Medical DevicesFDA
Olympus Corporation of the Americas recalls Bronchovideoscope BF-P180
Hazard: The attachment of non-Olympus accessories to the bronchoscope s instrument channel port may have resulted in more applied force than expected and lead to loosening of the instrument channel port.
October 10, 2018Medical DevicesFDA
Olympus Corporation of the Americas recalls Bronchovideoscope BF-P160
Hazard: The attachment of non-Olympus accessories to the bronchoscope s instrument channel port may have resulted in more applied force than expected and lead to loosening of the instrument channel port.
October 10, 2018Medical DevicesFDA
Olympus Corporation of the Americas recalls Bronchovideoscope BF-MP60
Hazard: The attachment of non-Olympus accessories to the bronchoscope s instrument channel port may have resulted in more applied force than expected and lead to loosening of the instrument channel port.
October 10, 2018Medical DevicesFDA
Olympus Corporation of the Americas recalls Bronchovideoscope BF-MP160F
Hazard: The attachment of non-Olympus accessories to the bronchoscope s instrument channel port may have resulted in more applied force than expected and lead to loosening of the instrument channel port.
October 10, 2018Medical DevicesFDA
Olympus Corporation of the Americas recalls Bronchofibercope BF-6C240
Hazard: The attachment of non-Olympus accessories to the bronchoscope s instrument channel port may have resulted in more applied force than expected and lead to loosening of the instrument channel port.
October 10, 2018Medical DevicesFDA
Olympus Corporation of the Americas recalls Bronchofiberscope BF-40
Hazard: The attachment of non-Olympus accessories to the bronchoscope s instrument channel port may have resulted in more applied force than expected and lead to loosening of the instrument channel port.
October 10, 2018Medical DevicesFDA
Olympus Corporation of the Americas recalls Bronchovideoscope BF-3C40
Hazard: The attachment of non-Olympus accessories to the bronchoscope s instrument channel port may have resulted in more applied force than expected and lead to loosening of the instrument channel port.
October 10, 2018Medical DevicesFDA
Olympus Corporation of the Americas recalls Bronchovideoscope BF-3C160
Hazard: The attachment of non-Olympus accessories to the bronchoscope s instrument channel port may have resulted in more applied force than expected and lead to loosening of the instrument channel port.