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.