Olympus recalls OER-ELITE Endoscope Reprocessor Connecting Tubes (model MAJ-2112) 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-2112 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.
Medical professionals using Olympus OER-ELITE Endoscope Reprocessor Connecting Tubes with model MAJ-2112 are most at risk. The recall affects specific lot numbers produced between 2009 and 2021.
Check for the model number MAJ-2112 on the connecting tube. Affected units have specific lot numbers ranging from 09A to 51A as listed in the recall notice.
Look for the lot number on the connecting tube, which should be one of the listed codes (09A through 51A).
No, the recall does not require immediate discontinuation. The hazard is low risk and only affects specific lot numbers.
Check the lot number on your connecting tube. If it matches the listed codes (09A through 51A), contact Olympus for further instructions.
The affected units have model number MAJ-2112 and lot numbers from 09A to 51A as specified in the recall notice.
We’ve drafted a message you can send Olympus to request your refund or repair — edit it as you like.
Subject: Recall Z-1900-2026 — Olympus Olympus Hello, I own a Olympus that is covered by recall Z-1900-2026 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.
