Olympus Inner 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 inner sheaths for urological and gynecological procedures because users have reported the ceramic tip breaking. This could lead to complications during medical procedures if the sheath breaks unexpectedly.

Why it’s dangerous

The ceramic tip of the sheath can break during use, potentially causing complications like bleeding or injury during medical procedures. This breakage is reported by users but does not indicate immediate danger in normal use.

Who’s affected

Healthcare providers using Olympus Inner Sheath, Long (model WA22017A) for urological and gynecological procedures are most at risk. Patients receiving these procedures may also be affected.

How to tell if you have this one

Check for the model number WA22017A on the sheath. The product is sold for urological and gynecological procedures and was manufactured with the UDI 04042761051514.

Brand
Olympus
Category
Medical device

Based on the official FDA remedy

What to do — step by step

Check Product Model
Verify the model number on the sheath is WA22017A.

✎ GovInfoNow

Questions people ask

Why is this sheath being recalled?

The recall is due to complaints about the ceramic tip breaking during use, which could cause complications in medical procedures.

Is there a fix for this sheath?

The official recall record does not mention a remedy or replacement.

How can I tell if I have the recalled sheath?

Look for the model number WA22017A on the sheath, which is used for urological and gynecological procedures.

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-1450-2026 — Olympus Olympus

Hello,

I own a Olympus that is covered by recall Z-1450-2026 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-1450-2026 (November 11, 2025) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for Z-1450-2026 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 Inner Sheath, Long; Model No. WA22017A. Inner sheath for urological and gynecological applications.

Lower-risk recall