Olympus recalls Bronchovideoscope BF-1T180 models due to potential loosening of the instrument channel port when non-Olympus accessories are attached. All lot codes are affected.
The attachment of non-Olympus accessories to the bronchoscope s instrument channel port may have resulted in more applied force than expected and lead to loosening of the instrument channel port.
Olympus is recalling its Bronchovideoscope BF-1T180 models because attaching non-Olympus accessories might cause the instrument channel port to loosen. This could lead to safety issues during medical procedures.
The instrument channel port can loosen when non-Olymp: Olympus accessories are attached, potentially causing the device to malfunction during medical procedures. This could lead to safety risks for both the user and the patient.
Healthcare professionals using the Bronchovideoscope BF-1T180 are most at risk, particularly when attaching non-Olympus accessories. Patients undergoing procedures with this device may also be affected.
Check for the Bronchovideoscope BF-1T180 model with any lot code. The product is sold by Olympus Corporation of the Americas.
Inspect the instrument channel port for signs of looseness after attaching non-Olympus accessories.
The recall affects healthcare professionals using the device, but patients undergoing procedures with the Bronchovideoscope BF-1T180 may be at risk if the device malfunctions.
The Bronchovideoscope BF-1T180 with any lot code is affected. Check the product label for the model and lot code.
Inspect the instrument channel port for looseness after attaching non-Olympus accessories. If loose, stop using the device until it is fixed.
We’ve drafted a message you can send Olympus to request your refund or repair — edit it as you like.
Subject: Recall Z-3285-2018 — Olympus Olympus Hello, I own a Olympus that is covered by recall Z-3285-2018 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.
