Olympus Announces Voluntary Corrective Action for the Single-Use Ligating Device

OtherMedical device
Date
Dec 5, 2025
Company
Olympus Corporation
Brand
Olympus
Product
Single use ligating device
Reason
PolyLoop device may fail to detach as expected and become anchored to patient anatomy
Hazard
Other
Source
FDA

Official notice (FDA)

Facts are taken from the official notice. If anything here differs from it, the official notice is correct.