Olympus recalls OER-ELITE Endoscope Reprocessor Connecting Tubes (Model MAJ-2116) due to potential lock lever failure. Affected units include specific lot numbers. Consumers should contact Olympus for details.
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-2116 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 Version 2 reprocessor 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 in normal use.
Healthcare professionals using the OER-ELITE Endoscope Reprocessor Connecting Tubes with model MAJ-2116 are most at risk. Patients using these tubes during medical procedures may be affected if the lock levers fail.
Check the model number on the tube, which should be MAJ-2116. Look for lot numbers listed: 09A, 0XA, 0YA, 0ZA, 11A, 25A, 26A, 27A, 28A, 45A, 46A, 47A, 48A, 49A, 4XA, 4YA, 51A.
Verify the model number is MAJ-2116 on the connecting tube.
Reach out to Olympus Corporation of the Americas for specific instructions on the recall.
The model number is MAJ-2116.
Affected lot numbers include 09A, 0XA, 0YA, 0ZA, 11A, 25A, 26A, 27A, 28A, 45A, 46A, 47A, 48A, 49A, 4XA, 4YA, 51A.
The recall does not require immediate stop use; contact Olympus for specific instructions.
We’ve drafted a message you can send Olympus to request your refund or repair — edit it as you like.
Subject: Recall Z-1904-2026 — Olympus Olympus Hello, I own a Olympus that is covered by recall Z-1904-2026 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.
