Home/Recalls/FDA-Z-1898-2026
FDA DevicesClass II

OER-ELITE Endoscope Reprocessor Connecting Tubes. Model/Catalog Number: MAJ-2110...

Published: April 29, 2026Recall ID: Z-1898-2026Category: devicesCountry: US

Reason for Recall / Hazard

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

Product Description & Identification

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

Affected Products

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

Additional Source Details

FieldValue
CityCenter Valley
StatePA
Event id98544
Address 13500 Corporate Pkwy
Address 2N/A
Code infoModel Number: MAJ-2110. UDI Number: 04953170404054. 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.
Postal code18034-8229
Report date20260429
Product typeDevices
Product quantity9,757 units
Reason for recallPotential for the Version 2 reprocessor connecting tube lock levers may fail prematurely.
Voluntary mandatedVoluntary: Firm initiated
Recall initiation date20260325
Initial firm notificationLetter
Center classification date20260422

Overview

  • Recalling FirmOlympus Corporation of the Americas
  • StatusOngoing
  • Risk LevelClass II
  • DistributionWorldwide distribution - US Nationwide and the countries of Canada, China, Hong Kong, Japan, South Korea and Taiwan.
Official Agency Alert