Olymp: Olympus recalls 24 Fr. resection sheaths with ceramic tip that may break during use, posing a potential injury risk for urologic procedures.
Complaints of the ceramic tip of the resection sheath breaking have been received.
Olympus is recalling urologic resection sheaths with model number A22041T due to complaints of ceramic tips breaking. This could lead to injury during medical procedures if the broken piece causes damage.
The ceramic tip of the resection sheath can break during use, potentially causing injury to the patient or medical staff. This breakage may occur during urologic procedures and could lead to complications if the broken piece is not properly managed.
Medical professionals using the Olympus Resection Sheath (24 Fr., Model A22041T) for urologic procedures are most at risk. Patients receiving these procedures may also be affected if the sheath breaks during surgery.
Check for the model number A22041T on the sheath. The product is sold for urologic applications and was manufactured with a unique identifier (UDI: 04042761020978). All lots are affected.
Inspect the sheath for any signs of ceramic tip breakage before use.
The Olympus Resection Sheath (Model A22041T) has been recalled due to complaints of ceramic tip breakage, so it is not recommended for use until the recall is addressed.
Look for the model number A22041T on the sheath. The product is sold for urologic applications and has a unique identifier (UDI: 04042761020978). All lots are affected.
The recall does not specify a remedy, so check with Olympus for guidance on handling the product if it is broken.
We’ve drafted a message you can send Olympus to request your refund or repair — edit it as you like.
Subject: Recall Z-1442-2026 — Olympus Olympus Hello, I own a Olympus that is covered by recall Z-1442-2026 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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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.
