Olympus A2660 Inner Sheath Recall: Ceramic Tip Breakage Risk

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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 A2660 Inner Sheath for endoscopic urological procedures because ceramic tips have broken. This could lead to complications during medical procedures if the sheath fails unexpectedly.

Why it’s dangerous

The ceramic tip of the sheath can break during use, potentially causing the sheath to malfunction. This could lead to complications during endoscopic procedures if the broken tip obstructs the procedure or causes tissue damage.

Who’s affected

Urology professionals using the Olympus A2660 Inner Sheath for endoscopic procedures are affected. The risk is low as breakage is reported but not confirmed to cause serious injury.

How to tell if you have this one

Check for the model number A2660 on the sheath. The unique device identifier (UDI) is 04042761004176. All lots of this product are affected.

Brand
Olympus
Category
Medical device

Based on the official FDA remedy

What to do — step by step

Check Product Details
Look for the model number A2660 and UDI 04042761004176 on the sheath.

✎ GovInfoNow

Questions people ask

Is this product safe to use?

The recall is due to reported ceramic tip breakage, but the product is not confirmed to cause serious injury. Use with caution.

How can I tell if I have the recalled product?

Check for the model number A2660 and UDI 04042761004176 on the sheath. All lots are affected.

What should I do if I have this product?

The recall does not specify a remedy, so contact Olympus Corporation of the Americas 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-1447-2026 — Olympus Olympus

Hello,

I own a Olympus that is covered by recall Z-1447-2026 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-1447-2026 (November 11, 2025) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for Z-1447-2026 to see it in context.
Plain-language summary written by qwen3:4b on August 10, 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 Inner Sheath; Model No. A2660. for endoscopic diagnosis and treatment in urological applications.

Lower-risk recall