Olympus Corporation of the Americas recalls Olympus Endoscope Reprocessor OER-Pro.
- Recalling company
- Olympus Corporation of the Americas
- Product
- Olympus Endoscope Reprocessor OER-Pro. Model Number: N3058140.
- Reason
- The MAJ-1443 and MAJ-1444 are no longer reprocessing compatible with the OER-Pro and OER-Elite automated endoscope reprocessors.
- Classification
- Class II – may cause temporary or medically reversible health consequences
- Recall date
- Feb 12, 2026
- Reported
- Apr 1, 2026
- Distribution
- US Nationwide distribution.
- Status
- Ongoing
- Quantity
- 3,354 units
- Lot / codes
- Model Number: N3058140. UDI-DI: 04953170258589. Catalog Number: N3058140. All Lot/Serial Numbers.
- Company location
- Center Valley, PA
- Recall type
- Voluntary: Firm initiated
- Recall number
- Z-1613-2026
- Agency
- U.S. Food and Drug Administration (FDA)
View official FDA notice ↗ Search recall number Z-1613-2026 in the FDA Enforcement Report. Also see FDA recall press releases.
If you use this product, check the lot, NDC or model number against the official notice and follow its instructions. Do not stop a prescribed medicine or remove a medical device without talking to your doctor or pharmacist. Report problems to FDA MedWatch. FoodRecallNow summarizes public FDA data and is not medical advice.