Class II
Medical Device Recall: Olympus OER-Elite
Aizu Olympus Co., Ltd. · October 31, 2025
Reason for Recall
Inform existing affected device customers about pertinent Warnings/Cautions, existing recommended maintenance schedules and that only properly trained personnel conduct repairs and maintenance.
Distribution
US Nationwide distribution.
States Affected
NATIONWIDE
Quantity Affected
6578 units
Source: FDA (openFDA Device Enforcement)
Recall number: Z-0872-2026
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.