Class II

Medical Device Recall: Olympus OER-Mini

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-0874-2026

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.