FDA Recall Open, Classified

Olympus OER-Mini

Recall: Z-0874-2026 · Initiated October 31, 2025

Recall

Recall Number
Z-0874-2026
Event Number
97849
Firm
Aizu Olympus Co., Ltd. 3 Chome 1-1 Niiderakita Aizuwakamatsu Japan
FEI Number
3002964398
Product Code
FEB
Status
Open, Classified
Root Cause
Under Investigation by firm
Initiated
October 31, 2025
Posted
December 2, 2025

Description

Olympus OER-Mini

Reason

Inform existing affected device customers about pertinent Warnings/Cautions, existing recommended maintenance schedules and that only properly trained personnel conduct repairs and maintenance.

Action

On October 31, 2025 URGENT Medical Device Safety Alert letters were sent to customers. Actions to be taken: 1. Olympus reminds users to follow the Warnings/Cautions and inspections outlined in all Olympus Endoscope Reprocessor Operation Manuals which are important to reduce the potential risk of fire to the device. 2. Carefully read the content of the notification. 3. Check your inventory for the reference devices and identify any in your inventory. 4. Ensure all personnel are completely knowledgeable and thoroughly aware of the contents of the letter. 5. Acknowledge receipt through the provided information. 6. Forward this notice if any affected product was further distributed.

Distribution

US Nationwide distribution.

Quantity

6578 units