Olympus recalls OER-Pro reprocessors with model N3058140 due to incompatibility with MAJ-1443/1444 endoscope reprocessing units. Affected units may not function correctly.
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 with model number N3058140 because they are no longer compatible with newer MAJ-1443 and MAJ-1444 reprocessing units. This could cause improper cleaning or infection risks if used with incompatible models.
The OER-Pro reprocessor can't properly handle the newer MAJ-1443 and MAJ-1444 endoscope reprocessing units. This may lead to incomplete cleaning or improper sterilization, potentially increasing infection risks.
Healthcare facilities using Olympus OER-Pro reprocessors with model N3058140 may be affected. Staff handling endoscopes in hospitals or clinics are most at risk if they use incompatible reprocessing units.
Check for model number N3058140 on the reprocessor. The UDI-DI code 04953170258589 and catalog number N3058140 are also associated with this recall.
Verify if your reprocessor works with MAJ-1443 or MAJ-1444 units by checking the model number and UDI-DI code.
The OER-Pro reprocessor is no longer compatible with newer MAJ-1443 and MAJ-1444 endoscope reprocessing units, which could lead to improper cleaning or infection risks.
No, the recall does not require immediate discontinuation. You can check compatibility with newer units to ensure proper function.
Check if your reprocessor works with MAJ-1443 or MAJ-1444 units. If not, contact Olympus for guidance on compatible alternatives.
We’ve drafted a message you can send Olympus to request your refund or repair — edit it as you like.
Subject: Recall Z-1613-2026 — Olympus Olympus Hello, I own a Olympus that is covered by recall Z-1613-2026 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.
