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FDA DeviceClass IINotable

FDA Recall: Olympus Inner Sheath. Model No. A4741. for endoscopic diagnosis and treatment in gynecological appl

Date: 2026-03-04
Brand: Olympus Corporation of the Americas
Category: Medical Device
FDA Class: Class II

Description

Complaints of the ceramic tip of the resection sheath breaking have been received.

Hazard

Complaints of the ceramic tip of the resection sheath breaking have been received.

Remedy

91 units

View original recall →
FDA Recall: Olympus Inner Sheath. Model No. A4741. for endoscopic diagnosis and treatment in gynecological appl | RecallWatch