FDA DeviceClass IINotable

FDA Recall: Olympus Inner Sheath, Long; Model No. WA22017T. Inner sheath for urological and gynecological appli

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

1,141 units

View original recall →
Share:

Related Recalls

2026-04-29 · FDA_DEVICE
FDA Recall: Olympus Thunderbeat II Shears w/Ultrasonic Mode, 5mm, 45cm. Model Number: TB2-0545FC.
Olympus Corporation of the Americas
2026-04-29 · FDA_DEVICE
FDA Recall: OER-ELITE Endoscope Reprocessor Connecting Tubes. Model/Catalog Number: MAJ-2115.
Olympus Corporation of the Americas
2026-04-29 · FDA_DEVICE
FDA Recall: OER-ELITE Endoscope Reprocessor Connecting Tubes. Model/Catalog Number: MAJ-2330.
Olympus Corporation of the Americas
2026-04-29 · FDA_DEVICE
FDA Recall: Olympus Thunderbeat II Shears w/Ultrasonic Mode, 5mm, 20cm. Model Number: TB2-0520FC.
Olympus Corporation of the Americas