Olympus recalls OER-ELITE Endoscope Reprocessor Connecting Tubes (model MAJ-2119) due to potential premature failure of lock levers. Affected units include specific lot numbers from 09A to 51A.
Potential for the Version 2 reprocessor connecting tube lock levers may fail prematurely.
Olympus is recalling OER-ELITE Endoscope Reprocessor Connecting Tubes with model number MAJ-2119 because the lock levers might fail prematurely. This could lead to improper connections during medical procedures. Affected units have specific lot numbers listed in the recall.
The lock levers in the connecting tubes may fail prematurely, potentially causing improper connections during medical procedures. This could lead to equipment malfunction but does not pose an immediate risk of injury or serious harm under normal use conditions.
Healthcare professionals using the OER-ELITE Endoscope Reprocessor Connecting Tubes with model MAJ-2119 are most at risk. The recall affects specific lot numbers produced between 2009 and 2023.
Check the model number on the tube, which should be MAJ-2119. The lot numbers range from 09A to 51A as listed in the recall notice.
Verify the model number is MAJ-2119 on the connecting tube.
Reach out to Olympus Corporation of the Americas for further assistance or to confirm if your unit is affected.
The model number is MAJ-2119.
Affected lot numbers range from 09A to 51A as listed in the recall notice.
No immediate action is required; the recall is for potential premature failure of lock levers, which does not pose an immediate risk of injury.
We’ve drafted a message you can send Olympus to request your refund or repair — edit it as you like.
Subject: Recall Z-1907-2026 — Olympus Olympus Hello, I own a Olympus that is covered by recall Z-1907-2026 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.
Experiences, tips, and questions from readers. Every comment is reviewed before it appears.
No comments yet — be the first to share your experience.
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.