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Medium risk Medical DevicesClass II

Olympus OER-ELITE Endoscope Tubes Recall

OER-ELITE Endoscope Reprocessor Connecting Tubes. Model/Catalog Number: MAJ-2115.

Updated March 25, 2026

Olympus has recalled OER-ELITE Endoscope Reprocessor Connecting Tubes (Model MAJ-2115) due to a defect that could affect proper sterilization and reprocessing of medical endoscopes. This may pose a risk of infection or contamination during medical procedures.

Is the Olympus Corporation of the Americas recalled? Yes. This product was recalled by FDA on March 25, 2026. Details below.

What is recalled

OER-ELITE Endoscope Reprocessor Connecting Tubes, Model/Catalog Number MAJ-2115, manufactured by Olympus Corporation of the Americas.

Am I affected

You're affected if you operate or maintain an OER-ELITE Endoscope Reprocessor and have connecting tubes with Model Number MAJ-2115 in use.

What to do right now

Stop using the affected connecting tubes immediately. Contact Olympus Corporation of the Americas for instructions on replacement or repair of your Model MAJ-2115 tubes.

The hazard

XXX

Brands affected

Olympus Corporation of the Americas
Source
FDA
Category
Medical Devices
Recall ID
fda-Z-1903-2026
Classification
Class II
Recalled
March 25, 2026
Read the official notice

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