medical MODERATE Updated 2026-04-01

Olympus Corporation of the Americas recalls Olympus Endoscope Reprocessor OER-Pro. Model Number: N305814

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Recalled Product

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

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Hazard / Issue

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

Issued by

FDA

Distribution: Nationwide (United States)
Lot/Code Info: Model Number: N3058140. UDI-DI: 04953170258589. Catalog Number: N3058140. All Lot/Serial Numbers.

✅ What Should You Do?

  1. 1Contact your healthcare provider immediately to discuss this recall.
  2. 2Stop using the device if it is safe to do so, and contact your provider.
  3. 3Follow the manufacturer's remedy instructions provided in the recall notice.
  4. 4Report device problems to FDA MedWatch or call 1-800-FDA-1088.

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