HomeMedical Device recalls
Medium severity

Olympus Resection Sheath. Model No. A2666T. for endoscopic diagnosis and treatment in urological 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

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