FDA DeviceClass IINotable
FDA Recall: Olympus Inner Sheath; Model No. A2660. for endoscopic diagnosis and treatment in urological applicat
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
9 units
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