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Aizu Olympus Co., Ltd.: Olympus OER-Mini

Medical DevicesSource: FDA (device) · Date: 2025-12-10

Read the official notice at FDA (device) →

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The text below is copied from the official FDA (device) record. If anything differs, the official notice is correct.

Company / brand
Aizu Olympus Co., Ltd.
Product
Olympus OER-Mini
Reason / hazard
Inform existing affected device customers about pertinent Warnings/Cautions, existing recommended maintenance schedules and that only properly trained personnel conduct repairs and maintenance.
Classification
Class II
Status
Ongoing
Distribution / sold at
US Nationwide distribution.
Recall initiated
2025-10-31
Code info
Model: OER-Mini; UDI: 04953170331619; Serial #: All;
Product quantity
6578 units
Voluntary mandated
Voluntary: Firm initiated
City
Aizuwakamatsu
Country
Japan
Event id
97849
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