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Z-1450-2026Class II
Olympus Corporation of the Americas
What this record is not
A recall record is reproduced as FDA published it, and the classification is FDA’s. SPEQ adds no interpretation, and a recall concerns the products and dates in the record — it is not a statement about a company’s other products or its current status.
Recalling firm
Olympus Corporation of the Americas
Product type
Device
Status
Ongoing
Report date
2026-03-04
Distribution
US Nationwide Distribution.
Firm state
PA
Product quantity
437 units
Initiated by
Voluntary: Firm initiated
Reason for recall
Complaints of the ceramic tip of the resection sheath breaking have been received.
Product description
Olympus Inner Sheath, Long; Model No. WA22017A. Inner sheath for urological and gynecological applications.
Code / lot info
Model No. WA22017A; UDI: 04042761051514; All Lots.
Data: U.S. FDA. Recall details are as reported by the FDA. The quality-domain mapping and severity are a SPEQ editorial interpretation of the recall reason, not an official FDA classification. Open the enforcement explorer →