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Recall Observatory FDA recall evidence

Device product

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

Z-1449-2026

November 11, 2025

Class II

Product summary

Firm
Olympus Corporation of the Americas
Event
Event 98288
Status
Ongoing
Classification
Class II
Quantity
91 units
Official record key
device-enforcement:Z-1449-2026

Official wording

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

Code information: Model No. A4741; UDI: 04042761006514; All Lots.

Distribution pattern: US Nationwide Distribution.

Derived failure modes

  • Unknown

    reason.no_named_rule · v1.0.0

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