Olympus recalls Ultrasonic Bronchoscope BF-UC180F 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 Ultrasonic Bronchoscope BF-UC180F models because attaching non-Olympus accessories could cause the instrument channel port to loosen. This poses a risk of injury during medical procedures if the port becomes loose.
The hazard occurs when non-Olympus accessories are attached to the instrument channel port. This can apply more force than expected, potentially loosening the port and causing injury during medical procedures.
Healthcare professionals using the Olympus Ultrasonic Bronchoscope BF-UC180F are most at risk. Patients undergoing procedures with this device may also be affected if the port loosens during use.
Check for the Olympus Ultrasonic Bronchoscope BF-UC180F model with any lot code. The product is sold under the brand name Olympus.
Inspect the instrument channel port for signs of loosening or damage after attaching non-Olympus accessories.
The attachment of non-Olympus accessories to the instrument channel port may apply more force than expected, leading to loosening of the port.
The recall does not specify a remedy, so check the instrument channel port for loosening after attaching non-Olympus accessories.
Yes, if the instrument channel port loosens during use, it could cause injury during medical procedures.
We’ve drafted a message you can send Olympus to request your refund or repair — edit it as you like.
Subject: Recall Z-3304-2018 — Olympus Olympus Hello, I own a Olympus that is covered by recall Z-3304-2018 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.
