FreshRecalls

OER-ELITE Endoscope Reprocessor Connecting Tubes: recall status

⚠ Recall found. OER-ELITE Endoscope Reprocessor Connecting Tubes is named in 12 official recalls in our current data. Details and the official notices are below — act on the remedy in the official notice.

Brand
Olympus of the Americas

Recalls naming this model

FDA Class II · Medical device · April 29, 2026

OER-ELITE Endoscope Reprocessor Connecting Tubes recall — Olympus Corporation of the Americas

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

Official ID Z-1898-2026 · Official record ↗

FDA Class II · Medical device · April 29, 2026

OER-ELITE Endoscope Reprocessor Connecting Tubes recall — Olympus Corporation of the Americas

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

Official ID Z-1899-2026 · Official record ↗

FDA Class II · Medical device · April 29, 2026

OER-ELITE Endoscope Reprocessor Connecting Tubes recall — Olympus Corporation of the Americas

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

Official ID Z-1900-2026 · Official record ↗

FDA Class II · Medical device · April 29, 2026

OER-ELITE Endoscope Reprocessor Connecting Tubes recall — Olympus Corporation of the Americas

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

Official ID Z-1901-2026 · Official record ↗

FDA Class II · Medical device · April 29, 2026

OER-ELITE Endoscope Reprocessor Connecting Tubes recall — Olympus Corporation of the Americas

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

Official ID Z-1902-2026 · Official record ↗

FDA Class II · Medical device · April 29, 2026

OER-ELITE Endoscope Reprocessor Connecting Tubes recall — Olympus Corporation of the Americas

XXX

Official ID Z-1903-2026 · Official record ↗

FDA Class II · Medical device · April 29, 2026

OER-ELITE Endoscope Reprocessor Connecting Tubes recall — Olympus Corporation of the Americas

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

Official ID Z-1904-2026 · Official record ↗

FDA Class II · Medical device · April 29, 2026

OER-ELITE Endoscope Reprocessor Connecting Tubes recall — Olympus Corporation of the Americas

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

Official ID Z-1905-2026 · Official record ↗

FDA Class II · Medical device · April 29, 2026

OER-ELITE Endoscope Reprocessor Connecting Tubes recall — Olympus Corporation of the Americas

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

Official ID Z-1906-2026 · Official record ↗

FDA Class II · Medical device · April 29, 2026

OER-ELITE Endoscope Reprocessor Connecting Tubes recall — Olympus Corporation of the Americas

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

Official ID Z-1907-2026 · Official record ↗

FDA Class II · Medical device · April 29, 2026

OER-ELITE Endoscope Reprocessor Connecting Tubes recall — Olympus Corporation of the Americas

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

Official ID Z-1908-2026 · Official record ↗

FDA Class II · Medical device · April 29, 2026

OER-ELITE Endoscope Reprocessor Connecting Tubes recall — Olympus Corporation of the Americas

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

Official ID Z-1909-2026 · Official record ↗

See all Olympus of the Americas recalls →

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Compiled from official public-domain CPSC, NHTSA, and FDA data. Sources last checked July 24, 2026 at 3:00 AM UTC.