Home/Recalls/FDA-Z-1610-2026
FDA DevicesClass II

Olympus Endoscope Suction Valve - MAJ-1443. Model Number: MAJ-1443.

Published: April 1, 2026Recall ID: Z-1610-2026Category: devicesCountry: US

Reason for Recall / Hazard

The MAJ-1443 and MAJ-1444 are no longer reprocessing compatible with the OER-Pro and OER-Elite automated endoscope reprocessors.

Product Description & Identification

Olympus Endoscope Suction Valve - MAJ-1443. Model Number: MAJ-1443.

Additional Source Details

FieldValue
CityCenter Valley
StatePA
Event id98371
Address 13500 Corporate Pkwy
Code infoModel Number: MAJ-1443. UDI-DI: 04953170355912. Catalog Number: N5363430. All Lot/Serial Numbers.
Postal code18034-8229
Report date20260401
Product typeDevices
Product quantity47,383 units
Reason for recallThe MAJ-1443 and MAJ-1444 are no longer reprocessing compatible with the OER-Pro and OER-Elite automated endoscope reprocessors.
Voluntary mandatedVoluntary: Firm initiated
Recall initiation date20260212
Initial firm notificationLetter
Center classification date20260320

Overview

  • Recalling FirmOlympus Corporation of the Americas
  • StatusOngoing
  • Risk LevelClass II
  • DistributionUS Nationwide distribution.
Official Agency Alert