Olympus recalls OER-ELITE Endoscope Reprocessor Connecting Tubes (Model MAJ-2114) 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-2114 because the lock levers might fail prematurely. This could lead to improper connection during medical procedures, potentially causing injury or equipment damage.
The lock levers in Version 2 reprocessor connecting tubes may fail prematurely, causing the tubes to disconnect unexpectedly during medical procedures. This could lead to equipment damage or injury to patients or staff.
Medical professionals using these connecting tubes in endoscopy procedures are most at risk. Patients and staff handling the equipment may also be affected if the lock levers fail during use.
Check for the model number MAJ-2114 on the connecting tubes. Affected units include specific lot numbers from 09A through 51A as listed in the recall notice.
Inspect the lock levers for signs of premature wear or damage that could cause the tubes to disconnect unexpectedly.
Reach out to Olympus Corporation of the Americas for specific instructions on how to verify if your unit is affected and what to do next.
Yes, affected lot numbers range from 09A to 51A as listed in the recall notice.
Contact Olympus Corporation of the Americas for specific instructions on how to verify if your unit is affected and what to do next.
The recall states potential for premature failure of lock levers, which could lead to equipment disconnection during procedures. However, the remedy does not specify immediate stop-use, so the risk level is use_caution.
We’ve drafted a message you can send Olympus to request your refund or repair — edit it as you like.
Subject: Recall Z-1902-2026 — Olympus Olympus Hello, I own a Olympus that is covered by recall Z-1902-2026 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.
