medtechdive2d
FDA labels recall of discontinued Olympus endoscope part as Class I
The update comes about six weeks after an early alert flagged reports of 120 injuries and one death linked to reprocessing of ...
Hosted on MSN1mon
FDA alerts users to issue with Olympus’s endoscope component after patient death
The US Food and Drug Administration (FDA) has issued an alert relating to a problem with a component on endoscopes manufactured by Olympus that may be “high-risk.” Olympus sent affected ...
USA Today10d
Olympus Issues Medical Device Advisory Notice to Use Alternative Devices to the MAJ-891 Forceps/Irrigation Plug
Olympus Corporation has announced a voluntary Advisory Notice for the Forceps/Irrigation Plug (Isolated Type) model MAJ-891 related to the risk of device contamination that may result from ...
Morningstar10d
Olympus Issues Medical Device Advisory Notice to Use Alternative Devices to the MAJ-891 Forceps/Irrigation Plug
The MAJ-891 is a reusable device and ... About Olympus At Olympus, we are committed to Our Purpose of making people's lives healthier, safer and more fulfilling. As a global medical technology ...
Olympus Issues Medical Device Advisory Notice to Use Alternative Devices to the MAJ-891 Forceps/Irrigation Plug
Olympus Corporation has announced a voluntary Advisory Notice for the Forceps/Irrigation Plug (Isolated Type) model MAJ-891 related to the risk of device contamination that may result from improper ...
Pharmabiz8d
Olympus issues medical device advisory notice to use alternative devices to the MAJ-891 accessory
Olympus issues medical device advisory notice to use alternative devices to the MAJ-891 accessory: Center Valley, Pennsylvania Friday, January 31, 2025, 11:00 Hrs [IST] Olympus Co ...