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Olympus Corporation of the Americas recalls Olympus Endoscope Reprocessor OER-Pro. Model Number: N3058140.
Recalled April 1, 2026 · FDA recall Z-1613-2026 · Olympus Corporation of the Americas
Hazard
The MAJ-1443 and MAJ-1444 are no longer reprocessing compatible with the OER-Pro and OER-Elite automated endoscope reprocessors. · FDA Class II
Units
3,354 units
Sold at
US Nationwide distribution.
Description
The MAJ-1443 and MAJ-1444 are no longer reprocessing compatible with the OER-Pro and OER-Elite automated endoscope reprocessors.
Product
Olympus Endoscope Reprocessor OER-Pro. Model Number: N3058140.
Manufacturer(s)
Olympus Corporation of the Americas
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →