Olympus recalls OER-Elite endoscope reprocessors (model N5789340) due to incompatibility with MAJ-1443/1444 reprocessing units. Affected units may not function correctly with newer reprocessing systems.
The MAJ-1443 and MAJ-1444 are no longer reprocessing compatible with the OER-Pro and OER-Elite automated endoscope reprocessors.
Olympus is recalling endoscope reprocessors (model N5789340) because they are no longer compatible with newer reprocessing units. This could cause improper cleaning and potential infection risks if used with incompatible systems.
The OER-Elite reprocessor (model N5789340) is designed to work with specific reprocessing units. When used with incompatible MAJ-1443 or MAJ-1444 units, it may not clean endoscopes properly, increasing infection risks.
Healthcare facilities using Olympus OER-Elite reprocessors with MAJ-1443 or MAJ-1444 reprocessing units are most affected. Patients using these systems may face infection risks if the reprocessing is incomplete.
Check for model number N5789340 on the reprocessor. The unit may have a UDI-DI code starting with 04953170404047. Affected units were sold with incompatible reprocessing units.
Verify if your OER-Elite reprocessor works with MAJ-1443 or MAJ-1444 reprocessing units by checking the model number and UDI-DI code.
The OER-Elite reprocessor (model N5789340) is no longer compatible with newer reprocessing units (MAJ-1443 and MAJ-1444), which could lead to improper cleaning and infection risks.
The recall does not require immediate action. Check if your reprocessor is compatible with MAJ-1443 or MAJ-1444 units before using it.
The official recall does not provide a fix. Affected users should ensure they are using compatible reprocessing units to avoid infection risks.
We’ve drafted a message you can send Olympus to request your refund or repair — edit it as you like.
Subject: Recall Z-1612-2026 — Olympus Olympus Hello, I own a Olympus that is covered by recall Z-1612-2026 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.
