HomeMedical Device recalls
Medium severity

Olympus Inner Sheath. Model No. A4741. for endoscopic diagnosis and treatment in gynecological applications.

SourceFDA Device Enforcement
CategoryMedical Device
SeverityMedium
Statusongoing
Recall dateNovember 11, 2025
ReportedMarch 04, 2026
Recalling firmOlympus Corporation of the Americas
Country / regionUnited States PA

Hazard

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

Affected products

Related recalls

Swan-Ganz Jr Catheter, Models: SGPT54, SGPT64P, SGPT755P · May 27, 2026Medtronic DLP Retrograde Cannula Manual-Inflate Silicone Body 15FR, Model 94215T; Cardiopulmonary bypass v · May 27, 2026Medtronic DLP Retrograde Cannula Manual-Inflate Silicone Body 15FR, Model 94665; Cardiopulmonary bypass va · May 27, 2026Swan-Ganz Catheter, Models: 131F7/131F7P, 131F7J, 141F7, 151F7, 834F75, 096F6/096F6P, C144F7, 782F75M, 132F5, · May 27, 2026Oncology Kit w/60" (152 cm) Appx 2.2 ml, Smallbore Ext Set w/ChemoLock Port, Clamp, Anti-Siphon Valve, Spiros; · May 27, 2026