Olympus recalls resection sheaths model A22040T due to reported ceramic tip breakage. Affected units include all lots sold with UDI 04042761029360.
Complaints of the ceramic tip of the resection sheath breaking have been received.
Olympus is recalling resection sheaths model A22040T for urologic use because ceramic tips have broken. This could cause injury during medical procedures if the broken piece gets stuck in the patient.
The ceramic tip can break during use, potentially getting stuck in the patient's body. This could cause injury if the broken piece remains lodged during surgery.
Urology surgeons and medical staff using the Olympus resection sheath model A22040T are affected. The risk is low as breakage is reported but not confirmed to cause serious injury.
Check for the model number A22040T on the sheath. All lots produced with UDI 04042761029360 are affected.
Look for model number A22040T and UDI 04042761029360 on the sheath packaging or label.
Yes, all lots with model number A22040T and UDI 04042761029360 are affected.
The recall record does not specify a remedy, so contact Olympus directly for guidance.
The recall mentions reported breakage but does not state that injuries have occurred or are likely to cause serious harm.
We’ve drafted a message you can send Olympus to request your refund or repair — edit it as you like.
Subject: Recall Z-1440-2026 — Olympus Olympus Hello, I own a Olympus that is covered by recall Z-1440-2026 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.
