Import Alerts for Certain Olympus Medical Devices ...
Jun 24, 2025 · Be aware of the FDA import alerts for certain medical devices manufactured in Japan by Olympus Medical Systems Corporation (Olympus) and its subsidiaries, under which the devices will …
Olympus Issues Voluntary Labeling Update for Bronchoscopes ...
Mar 11, 2025 · Since the Field Corrective Action in 2023, Olympus conducted additional assessment on the use of bronchoscopes with laser therapy, argon plasma coagulation, and high-frequency …
Olympus Issues Voluntary Recall for Specific Lots of ViziShot ...
Sep 22, 2025 · Health care personnel treating patients using an Olympus ViziShot 2 FLEX must ensure they are not using product from the affected lots, which are those manufactured prior to May 12, 2025.
Update on Alert: Endoscope Accessories Issue from Olympus
Mar 5, 2025 · The FDA is aware that Olympus has issued a letter to affected health care providers recommending the forceps/irrigation plug accessory to certain endoscopes be removed from use:
Correction Alert: Olympus Updates Use Instructions for ...
Dec 3, 2025 · Olympus received complaints indicating that the ligation loop was unable to release or detach as expected during use, causing the loop to become unintentionally anchored in place around …
Olympus Corporation of the Americas Recalls ...
Feb 28, 2024 · Olympus bronchoscopes, used to examine or treat a person's airways, are being recalled because they can lead to burns and fire.
Olympus Issues Medical Device Advisory Notice to Use ...
Jan 30, 2025 · 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 …