Olympus Resection Sheath Recall: 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

No email on file — write to the address above instead.

✎ GovInfoNow plain-language explainer

What happened, in plain English

Olympus is recalling resection sheaths for urologic use because ceramic tips may break. This could cause injury during medical procedures if the broken piece gets stuck in the patient.

Why it’s dangerous

The ceramic tip can break during use, potentially getting stuck in the patient's urinary tract. This could cause injury or require additional medical intervention.

Who’s affected

Urology surgeons and medical staff using the Olympus Resection Inner Sheath (Model A22040A) are affected. Patients undergoing procedures with this sheath are at risk if the ceramic tip breaks.

How to tell if you have this one

Check for the model number A22040A on the sheath. The product is sold as a resection sheath for urologic applications. All lots are affected.

Brand
Olympus
Category
Medical device

Based on the official FDA remedy

What to do — step by step

Check for Ceramic Tip Breakage
Inspect the sheath for any broken ceramic tips, especially near the end of the sheath.

✎ GovInfoNow

Questions people ask

Is this product safe to use?

The product may have a ceramic tip that breaks, so it's not safe to use without checking for damage.

How can I tell if I have the recalled product?

Look for the model number A22040A on the sheath. All lots are affected.

What should I do if I find a broken ceramic tip?

The recall does not specify a remedy for broken tips, so 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-1439-2026 — Olympus Olympus

Hello,

I own a Olympus that is covered by recall Z-1439-2026 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-1439-2026 (November 11, 2025) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for Z-1439-2026 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 Inner Sheath, for 26 Fr. Outer Sheath. Model No. A22040A. Resection sheath for urologic applications.

Use caution until it’s fixed