Reported Apr 29, 2026 · Ongoing

OER-ELITE Endoscope Reprocessor Connecting Tubes. Model/Catalog Number: MAJ-2110. May be included with the Olympus…

Olympus Corporation of the Americas

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

What you should do

Stop using the affected lot and contact the recalling firm for the return or refund process. Check the FDA enforcement report for lot-level detail.

Firm contact: Olympus Corporation of the Americas · 3500 Corporate Pkwy · Center Valley, PA · 18034-8229

Is this the product you have?

  • OER-ELITE Endoscope Reprocessor Connecting Tubes
  • Model/Catalog NumberMAJ-2110. May be included with the Olympus OER-ELITE
Lot codes and dates
  • Model NumberMAJ-2110
  • UDI Number04953170404054
  • Lot Numbers
    • 09A
    • 0XA
    • 0YA
    • 0ZA
    • 11A
    • 12A
    • 22A
    • 23A
    • 24A
    • 25A
    • 26A
    • 27A
    • 28A
    • 29A
    • 2XA
    • 2YA
    • 2ZA
    • 31A
    • 32A
    • 33A
    • 34A
    • 35A
    • 36A
    • 37A
    • 38A
    • 39A
    • 3XA
    • 3YA
    • 3ZA
    • 41A
    • 42A
    • 43A
    • 44A
    • 45A
    • 46A
    • 47A
    • 48A
    • 49A
    • 4XA
    • 4YA
    • 4ZA
    • 51A
Amount recalled
9,757 units

This recall covers 16 products

The agency filed one notice per product. You are reading one of them; the other 15 are below.

3 more are in the archive.

Where it was sold

  • Nationwide

Why it was recalled

Potential for the Version 2 reprocessor connecting tube lock levers may fail prematurely.

This product could cause temporary or reversible health problems — stop using it.

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Where this came from

Source: U.S. Food & Drug Administration (openFDA)

Read the FDA (openFDA device enforcement) notice

Data as of Sep 19, 4:16 PM UTC

RecallNow is not a government agency. Every fact on this page is published by the FDA, USDA or CPSC and links back to their notice.