Olympus recalls all Bronchofiberscope BF-P60 models due to risk of instrument channel port loosening from non-Olympus accessories. Affected units include all lot codes.
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 all Bronchofiberscope BF-P60 models because non-Olympus accessories might cause the instrument channel port to loosen. This could lead to potential injury during medical procedures.
Non-Olympus accessories attached to the instrument channel port can apply more force than expected, potentially loosening the port. This could cause injury during medical procedures if the port becomes dislodged.
Medical professionals using the Bronchofiberscope BF-P60 are most at risk. Patients undergoing procedures with this device may also be affected if non-Olympus accessories are used.
Check for the Bronchofiberscope BF-P60 model with any lot code. The product is sold by Olympus Corporation of the Americas.
Remove any non-Olympus accessories from the instrument channel port to prevent potential loosening.
The recall applies to the Bronchofiberscope BF-P60 used in medical procedures. If you have this device, check for non-Olympus accessories.
All Bronchofiberscope BF-P60 models with any lot code are affected. Check the product label for the model and lot code.
Remove any non-Olympus accessories from the instrument channel port to prevent potential loosening. Olympus does not provide a replacement or repair.
We’ve drafted a message you can send Olympus to request your refund or repair — edit it as you like.
Subject: Recall Z-3300-2018 — Olympus Olympus Hello, I own a Olympus that is covered by recall Z-3300-2018 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.
