OER-ELITE Endoscope Reprocessor Connecting Tubes: recall status
⚠ Recalls found. OER-ELITE Endoscope Reprocessor Connecting Tubes is named in 12 official recalls in our current data:
- Brand
- Olympus of the Americas
Recalls naming this model
FDA Class II · Medical device · April 29, 2026
Potential for the Version 2 reprocessor connecting tube lock levers may fail prematurely.
Company / brand: Olympus of the Americas
Affected product: OER-ELITE Endoscope Reprocessor Connecting Tubes
Official ID Z-1898-2026 ·
Official record ↗
FDA Class II · Medical device · April 29, 2026
Potential for the Version 2 reprocessor connecting tube lock levers may fail prematurely.
Company / brand: Olympus of the Americas
Affected product: OER-ELITE Endoscope Reprocessor Connecting Tubes
Official ID Z-1899-2026 ·
Official record ↗
FDA Class II · Medical device · April 29, 2026
Potential for the Version 2 reprocessor connecting tube lock levers may fail prematurely.
Company / brand: Olympus of the Americas
Affected product: OER-ELITE Endoscope Reprocessor Connecting Tubes
Official ID Z-1900-2026 ·
Official record ↗
FDA Class II · Medical device · April 29, 2026
Potential for the Version 2 reprocessor connecting tube lock levers may fail prematurely.
Company / brand: Olympus of the Americas
Affected product: OER-ELITE Endoscope Reprocessor Connecting Tubes
Official ID Z-1901-2026 ·
Official record ↗
FDA Class II · Medical device · April 29, 2026
Potential for the Version 2 reprocessor connecting tube lock levers may fail prematurely.
Company / brand: Olympus of the Americas
Affected product: OER-ELITE Endoscope Reprocessor Connecting Tubes
Official ID Z-1902-2026 ·
Official record ↗
FDA Class II · Medical device · April 29, 2026
XXX
Company / brand: Olympus of the Americas
Affected product: OER-ELITE Endoscope Reprocessor Connecting Tubes
Official ID Z-1903-2026 ·
Official record ↗
FDA Class II · Medical device · April 29, 2026
Potential for the Version 2 reprocessor connecting tube lock levers may fail prematurely.
Company / brand: Olympus of the Americas
Affected product: OER-ELITE Endoscope Reprocessor Connecting Tubes
Official ID Z-1904-2026 ·
Official record ↗
FDA Class II · Medical device · April 29, 2026
Potential for the Version 2 reprocessor connecting tube lock levers may fail prematurely.
Company / brand: Olympus of the Americas
Affected product: OER-ELITE Endoscope Reprocessor Connecting Tubes
Official ID Z-1905-2026 ·
Official record ↗
FDA Class II · Medical device · April 29, 2026
Potential for the Version 2 reprocessor connecting tube lock levers may fail prematurely.
Company / brand: Olympus of the Americas
Affected product: OER-ELITE Endoscope Reprocessor Connecting Tubes
Official ID Z-1906-2026 ·
Official record ↗
FDA Class II · Medical device · April 29, 2026
Potential for the Version 2 reprocessor connecting tube lock levers may fail prematurely.
Company / brand: Olympus of the Americas
Affected product: OER-ELITE Endoscope Reprocessor Connecting Tubes
Official ID Z-1907-2026 ·
Official record ↗
FDA Class II · Medical device · April 29, 2026
Potential for the Version 2 reprocessor connecting tube lock levers may fail prematurely.
Company / brand: Olympus of the Americas
Affected product: OER-ELITE Endoscope Reprocessor Connecting Tubes
Official ID Z-1908-2026 ·
Official record ↗
FDA Class II · Medical device · April 29, 2026
Potential for the Version 2 reprocessor connecting tube lock levers may fail prematurely.
Company / brand: Olympus of the Americas
Affected product: OER-ELITE Endoscope Reprocessor Connecting Tubes
Official ID Z-1909-2026 ·
Official record ↗
See all Olympus of the Americas recalls →
Compiled from connected official public-domain government data. Sources last checked September 7, 2026 at 6:00 AM UTC.