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 a specific inner sheath used in urological and gynecological procedures because complaints indicate the ceramic tip can break. This breakage could potentially cause injury during medical procedures.

Why it’s dangerous

The ceramic tip of the sheath can break during use, which may lead to injury or complications during medical procedures. This breakage is reported in complaints but the exact mechanism isn't specified.

Who’s affected

Healthcare professionals using the Olympus Inner Sheath model WA22017T for urological or 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 WA22017T on the sheath. The product was sold with a unique device identifier (UDI) 04042761051521. All production lots are affected.

Brand
Olympus
Category
Medical device

Based on the official FDA remedy

What to do — step by step

Check Product Details
Identify the model number on the sheath to confirm if it matches WA22017T.

✎ GovInfoNow

Questions people ask

Is there a fix for this issue?

The official recall notice does not state any remedy or fix for this issue.

How can I tell if I have the recalled product?

Look for the model number WA22017T on the sheath. The product was sold with a unique device identifier (UDI) 04042761051521 and all production lots are affected.

What should I do if I have the recalled product?

The official recall notice does not specify any action steps for affected users.

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-1451-2026 — Olympus Olympus

Hello,

I own a Olympus that is covered by recall Z-1451-2026 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-1451-2026 (November 11, 2025) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for Z-1451-2026 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. WA22017T. Inner sheath for urological and gynecological applications.

Recall notice