Olympus recalls specific colonoscopes (model CF-HQ190L) that may fail under vibration, temperature shifts, or shock due to missing adhesive. Affected units have unique serial numbers listed. Consumers should contact Olympus for details.
Specific repaired colonovideoscopes were assembled without an adhesive which protects them from certain physical conditions such as high levels of vibration, fluctuation in temperature or severe shock loads.
Olympus is recalling colonoscopes with model number CF-HQ190L that were assembled without a protective adhesive. This could cause the device to malfunction during procedures if exposed to high vibration, temperature changes, or physical shocks.
The colonoscopes were assembled without a protective adhesive that normally prevents damage from high vibration, temperature fluctuations, or severe shocks. If the device fails during use, it could cause injury or procedure interruption.
Medical professionals who use Olympus colonoscopes with model number CF-HQ190L are most at risk. Patients undergoing procedures with these specific models may experience device failure.
Check for the model number CF-HQ190L on the device. Affected units have specific serial numbers listed in the recall notice, including 2082724, 2082896, and other numbers provided in the recall.
Look for the model number CF-HQ190L on the colonoscope to determine if it is affected.
Reach out to Olympus Corporation of the Americas for specific guidance on affected units and next steps.
Yes, the recall includes specific serial numbers starting with 2082724, 2082896, and others listed in the notice.
The colonoscopes were assembled without a protective adhesive that prevents damage from vibration, temperature changes, or shocks during use.
No, the recall indicates a low risk of failure under normal conditions, but affected units should be checked with Olympus for guidance.
We’ve drafted a message you can send Olympus to request your refund or repair — edit it as you like.
Subject: Recall Z-1207-2024 — Olympus Olympus Hello, I own a Olympus that is covered by recall Z-1207-2024 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.
