Olympus recalls OER-ELITE Endoscope Reprocessor Connecting Tubes (Model MAJ-2113) due to potential premature failure of lock levers. Affected units include specific lot numbers and may require replacement.
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-2113 because the lock levers might fail prematurely. This could lead to improper connections during medical procedures, potentially causing safety issues.
The lock levers in the connecting tubes may fail prematurely, which could result in improper connections during medical procedures. This might cause the tubes to disconnect unexpectedly, potentially leading to safety issues.
Healthcare professionals using these connecting tubes in medical procedures are most at risk. The recall affects specific lot numbers produced between 2009 and 2024.
Check the model number on the tube, which should be MAJ-2113. Affected units include specific lot numbers listed in the recall notice (e.g., 09A, 11A, 22A, etc.).
Verify the model number on the connecting tube is MAJ-2113.
Reach out to Olympus Corporation of the Americas for assistance with the recall.
The model number is MAJ-2113.
Affected lot numbers include 09A, 0XA, 0YA, 0ZA, 11A, 12A, 22A, 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.
The recall does not require immediate stop use; affected users should check the model and lot numbers and contact Olympus for assistance.
We’ve drafted a message you can send Olympus to request your refund or repair — edit it as you like.
Subject: Recall Z-1901-2026 — Olympus Olympus Hello, I own a Olympus that is covered by recall Z-1901-2026 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.
