HomeMedical Device recalls
Medium severity

Olympus Endoscope Reprocessor OER-Pro. Model Number: N3058140.

SourceFDA Device Enforcement
CategoryMedical Device
SeverityMedium
Statusongoing
Recall dateFebruary 12, 2026
ReportedApril 01, 2026
Recalling firmOlympus Corporation of the Americas
Country / regionUnited States PA

Hazard

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

Affected products

Related recalls

Swan-Ganz Jr Catheter, Models: SGPT54, SGPT64P, SGPT755P · May 27, 2026Medtronic DLP Retrograde Cannula Manual-Inflate Silicone Body 15FR, Model 94215T; Cardiopulmonary bypass v · May 27, 2026Medtronic DLP Retrograde Cannula Manual-Inflate Silicone Body 15FR, Model 94665; Cardiopulmonary bypass va · May 27, 2026Swan-Ganz Catheter, Models: 131F7/131F7P, 131F7J, 141F7, 151F7, 834F75, 096F6/096F6P, C144F7, 782F75M, 132F5, · May 27, 2026Oncology Kit w/60" (152 cm) Appx 2.2 ml, Smallbore Ext Set w/ChemoLock Port, Clamp, Anti-Siphon Valve, Spiros; · May 27, 2026