Olymp: Olympus recalls EVIS EXERA b bronchovideoscope model BF-XT190 due to potential safety risks when used with laser and other equipment. Learn about the recall and what to do.
Additional IFU updates to provide further clarification on safe and effective use of bronchoscopes when used in conjunction with laser, argon plasma coagulation, and high-frequency therapy equipment.
Olympus is recalling its EVIS EXERA b bronchovideoscope model BF-XT190 because additional instructions are needed for safe use with laser and other medical equipment. This recall is important for healthcare providers to prevent potential safety issues during procedures.
The device requires updated instructions for safe use with laser, argon plasma coagulation, and high-frequency therapy equipment. Without these updates, there could be risks during medical procedures, though the hazard is not described as causing serious injury in normal use.
Healthcare providers using the Olympus EVIS EXERA b bronchovideoscope model BF-XT190 are likely affected. Patients undergoing procedures with this equipment may be at risk if the device is used incorrectly.
Check for the model number BF-XT190 on the device. The recall applies to all units sold by Olympus Corporation of the Americas.
Olympus will provide additional instructions for safe use with laser and other equipment. Check the manufacturer's website for the latest guidelines.
The recall states that additional instructions are needed for safe use with specific equipment, but it does not indicate that the device is dangerous in normal use.
Check for the model number BF-XT190 on the device. The recall applies to all units sold by Olympus Corporation of the Americas.
Olympus will provide updated instructions for safe use with laser and other equipment. No immediate action is required beyond reviewing the new instructions.
We’ve drafted a message you can send Olympus to request your refund or repair — edit it as you like.
Subject: Recall Z-0066-2026 — Olympus Olympus Hello, I own a Olympus that is covered by recall Z-0066-2026 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.
