Olympus Resection Sheath A2666T: Ceramic Tip Breakage Risk

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Contact the company & request your remedy

Recalling firmOlympus Corporation of the Americas3500 Corporate Pkwy, N/A · Center Valley, PA 18034-8229

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✎ GovInfoNow plain-language explainer

What happened, in plain English

Olympus is recalling its Resection Sheath model A2666T for urological procedures because ceramic tips have broken. This could cause injury during medical procedures if the broken piece becomes a hazard.

Why it’s dangerous

The ceramic tip can break during use, potentially causing injury to the patient or healthcare provider. Broken pieces could become sharp objects that cause cuts or other injuries during medical procedures.

Who’s affected

Healthcare professionals using the Olympus Resection Sheath model A2666T for urological procedures are most at risk. Patients receiving these procedures may also be affected if the sheath breaks during treatment.

How to tell if you have this one

Check for the model number A2666T on the sheath. Units sold with UDI 04042761004251 are affected. All lots of this model are included in the recall.

Brand
Olympus
Category
Medical device

Based on the official FDA remedy

What to do — step by step

Check for Breakage
Inspect the sheath for any signs of ceramic tip damage or breakage.
Contact Manufacturer
Reach out to Olympus Corporation of the Americas for guidance on next steps.

✎ GovInfoNow

Questions people ask

Is this sheath safe to use?

The recall indicates reported breakage, but the sheath is not currently being recalled for safety issues. Users should check for damage before use.

How can I tell if my sheath is affected?

Check for model number A2666T and UDI 04042761004251 on the sheath. All lots of this model are affected.

What should I do if the tip breaks?

The recall does not specify actions for broken tips. Contact Olympus for guidance.

Take action

Contact Olympus

We’ve drafted a message you can send Olympus to request your refund or repair — edit it as you like.

✉️ Open in email

Subject: Recall Z-1457-2026 — Olympus Olympus

Hello,

I own a Olympus that is covered by recall Z-1457-2026 from Olympus.

I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this?

Thank you.

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Where this comes from

The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.

Official source: FDA Recall #Z-1457-2026 (November 11, 2025) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for Z-1457-2026 to see it in context.
Plain-language summary written by qwen3:4b on August 18, 2026, from the official record above. Not reviewed by a person — if it conflicts with the FDA notice, the notice is correct. Report an error on this page.
GovInfoNow is an independent service and is not a government agency. We republish official FDA recall data; we don’t issue, amend or administer recalls.

Olympus Corporation of the Americas recalls Olympus Resection Sheath. Model No. A2666T. for endoscopic diagnosis and treatment in urological applications.

Use caution until it’s fixed