Aizu Olympus Co., Ltd.: Device Recall
Recall #Z-0873-2026 · 10/31/2025
Class II: Risk
Recall Details
- Recall Number
- Z-0873-2026
- Classification
- Class II
- Product Type
- Device
- Recalling Firm
- Aizu Olympus Co., Ltd.
- Status
- Ongoing
- Date Initiated
- 10/31/2025
- Location
- Aizuwakamatsu, Japan
- Voluntary/Mandated
- Voluntary: Firm initiated
- Product Quantity
- 6578 units
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.
Product Description
Olympus OER-Pro
Distribution Pattern
US Nationwide distribution.
Other Recalls by Aizu Olympus Co., Ltd.
- Class II: Risk 10/31/2025
- Class II: Risk 10/31/2025
Data from FDA openFDA enforcement reports. This site is not affiliated with or endorsed by the FDA. Recall information may be updated by the FDA at any time.