FDA DeviceClass IINotable

FDA Recall: Olympus Inner Sheath 21 Fr. Model No. A2660T. for endoscopic diagnosis and treatment in urological

Name: FDA Recall: Olympus Inner Sheath 21 Fr. Model No. A2660T. for endoscopic diagnosis and treatment in urological
Brand: Olympus Corporation of the Americas

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

1 unit

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