Olympus recalls specific models of tracheal intubation fiberscopes due to insufficient suction flow rates, potentially affecting medical procedures. Affected units include serial numbers listed in the recall notice.
Fiberscopes do not have adequate data to support that the suction flow rate meets the device specification.
Olympus is recalling certain tracheal intubation fiberscopes (model LF-GP) because they may not provide adequate suction flow rates as specified. This could impact medical procedures where precise suction is needed.
The fiberscopes may not meet the required suction flow rate specifications. This could lead to insufficient removal of fluids or debris during medical procedures, potentially affecting patient outcomes.
Healthcare professionals using the Olympus LF-GP fiberscopes are most at risk. Patients undergoing procedures with these devices may experience complications if suction flow is inadequate.
Check for the model number LF-GP on the device. Affected units have specific serial numbers listed in the recall notice, including 2515143, 2515181, and other numbers provided.
Compare your device's serial number with the list of affected numbers provided in the recall notice.
The fiberscopes may not provide adequate suction flow rates as specified, which could affect medical procedures.
Check your device's serial number against the list of affected numbers provided in the recall notice. If it matches, contact Olympus for further instructions.
The recall is due to potential inadequate suction flow rates, which could impact procedures but does not indicate immediate patient risk in normal use.
We’ve drafted a message you can send Olympus to request your refund or repair — edit it as you like.
Subject: Recall Z-0557-2024 — Olympus Olympus Hello, I own a Olympus that is covered by recall Z-0557-2024 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.
