Olympus recalls its Bronchovideoscope Olympus BF Type P150 due to potential safety risks when used with laser, argon plasma coagulation, and high-frequency therapy equipment. Affected units have specific model and serial numbers.
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 Bronchovideoscope Olympus BF Type P150 because additional safety instructions are needed when using it with certain medical equipment like lasers. This recall is important for healthcare providers to prevent potential risks during procedures.
The device requires updated safety instructions when used with specific medical equipment. Without these updates, there could be risks during procedures such as improper use leading to potential complications.
Healthcare professionals using the Olympus Bronchovideoscope P150 with laser, argon plasma coagulation, or high-frequency therapy equipment. Patients undergoing procedures with this device may be at risk if the safety updates are not followed.
Check for model number BF-P150 and serial numbers on the device. The recall includes all units with the unique device identifier (UDI) 4953170308178.
Identify the model number (BF-P150) and serial number on the device to confirm if it is affected.
Olympus is recalling the Bronchovideoscope Olympus BF Type P150 to provide additional safety instructions for use with laser, argon plasma coagulation, and high-frequency therapy equipment.
Check the model number and serial number on the device to see if it is affected. The recall includes all units with the unique device identifier (UDI) 4953170308178.
The recall provides updated safety instructions but does not include a repair or replacement option.
We’ve drafted a message you can send Olympus to request your refund or repair — edit it as you like.
Subject: Recall Z-0055-2026 — Olympus Olympus Hello, I own a Olympus that is covered by recall Z-0055-2026 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.
