Reported Mar 4, 2026 · Ongoing
Olympus Inner Sheath. Model No. A2642. for endoscopic diagnosis and treatment in urological applications.
Olympus Corporation of the Americas
Moderate riskThis product could cause temporary or reversible health problems — stop using it.What you should do
Stop using the affected lot and contact the recalling firm for the return or refund process. Check the FDA enforcement report for lot-level detail.
Firm contact: Olympus Corporation of the Americas · 3500 Corporate Pkwy · Center Valley, PA · 18034-8229
Is this the product you have?
- Olympus Inner Sheath. Model No. A2642. for endoscopic diagnosis and treatment in urological applications.
- Lot codes and dates
- Model No. A2642
- UDI04042761004084; All Lots
- Amount recalled
- 0 units
This recall covers 21 products
The agency filed one notice per product. You are reading one of them; the other 20 are below.
8 more are in the archive.
Where it was sold
- Nationwide
Why it was recalled
Complaints of the ceramic tip of the resection sheath breaking have been received.
This product could cause temporary or reversible health problems — stop using it.
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The guide adds the identifying codes laid out for scanning, symptoms to watch for, a timeline, and news coverage of this recall.
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