Olympus recalls OER-ELITE Endoscope Reprocessor Connecting Tubes (MAJ-2111) 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-2111 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 Version 2 reprocessor connecting tubes may fail prematurely, potentially causing improper connections during medical procedures. This could lead to equipment malfunction or incorrect use of the endoscope reprocessor.
Healthcare professionals using these connecting tubes in medical procedures are most at risk. Patients using the equipment may be affected if the tubes fail during treatment.
Check the model number on the tube, which should be MAJ-2111. Affected units include specific lot numbers from 09A to 51A as listed in the recall notice.
Look for the model number MAJ-2111 on the connecting tube.
The lock levers in the Version 2 reprocessor connecting tubes may fail prematurely, potentially causing improper connections during medical procedures.
Check the model number and lot number on the tube. If it matches the recalled model (MAJ-2111) and the listed lot numbers, contact Olympus for further instructions.
The recall is for potential premature failure of lock levers, which could lead to improper connections during medical procedures. However, the hazard is not described as causing serious injury in normal use.
We’ve drafted a message you can send Olympus to request your refund or repair — edit it as you like.
Subject: Recall Z-1899-2026 — Olympus Olympus Hello, I own a Olympus that is covered by recall Z-1899-2026 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.
