Class II

Medical Device Recall: Olympus Endoscope Reprocessor OER-Elite. Model Number: N5789340.

Olympus Corporation of the Americas · February 12, 2026

Reason for Recall

The MAJ-1443 and MAJ-1444 are no longer reprocessing compatible with the OER-Pro and OER-Elite automated endoscope reprocessors.

Distribution

US Nationwide distribution.

States Affected

NATIONWIDE

Quantity Affected

2,929 units

Source: FDA (openFDA Device Enforcement)

Recall number: Z-1612-2026

Status: ongoing

SafeCheck provides drug interaction information from FDA-approved product labeling (openFDA). This is for informational purposes only and is not medical advice. Always consult your healthcare provider before making medication decisions.

Olympus Corporation of the Americas Medical Device Recall: Olympus Endoscope Reprocessor OER-Elite. Model Number: N5789340. | SafeCheck