Olympus recalls OER-ELITE Endoscope Reprocessor Connecting Tubes (MAJ-2110) due to potential premature failure of lock levers. Affected units include specific lot numbers sold from 2009-2015.
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-2110 because the lock levers might fail prematurely. This could lead to improper connections during medical procedures. Affected units include specific lot numbers sold between 2009 and 2015.
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 indicate immediate danger to users.
Medical professionals using Olympus OER-ELITE Endoscope Reprocessor Connecting Tubes with model MAJ-2110 are most at risk. The recall affects specific lot numbers sold from 2009 to 2015.
Check for model number MAJ-2110 on the connecting tube. Affected units include specific lot numbers: 09A, 0XA, 0YA, 0ZA, 11A, 12A, 22A, 23A, 24A, 25A, 26A, 27A, 28A, 29A, 2XA, 2YA, 2ZA, 31A, 32A, 33A, 34A, 35A, 36A, 37A, 38A, 39A, 3XA, 3YA, 3ZA, 41A, 42A, 43A, 44A, 45A, 46A, 47A, 48A, 49A, 4XA, 4YA, 4ZA, 51A.
Look for model number MAJ-2110 on the connecting tube.
Reach out to Olympus Corporation of the Americas for assistance with the recall.
The recalled model number is MAJ-2110.
Affected lot numbers include 09A, 0XA, 0YA, 0ZA, 11A, 12A, 22A, 23A, 24A, 25A, 26A, 27A, 28A, 29A, 2XA, 2YA, 2ZA, 31A, 32A, 33A, 34A, 35A, 36A, 37A, 38A, 39A, 3XA, 3YA, 3ZA, 41A, 42A, 43A, 44A, 45A, 46A, 47A, 48A, 49A, 4XA, 4YA, 4ZA, 51A.
Check for model number MAJ-2110 and the specific lot numbers listed in the recall.
We’ve drafted a message you can send Olympus to request your refund or repair — edit it as you like.
Subject: Recall Z-1898-2026 — Olympus Olympus Hello, I own a Olympus that is covered by recall Z-1898-2026 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.
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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.
