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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 ...
FDA labels recall of discontinued Olympus endoscope accessory 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 the device.
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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 ...
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 ...