Changeflow GovPing Healthcare Olympus Biopsy Valve Recall Class II Z-1489-2026
Routine Notice Added

Olympus Biopsy Valve Recall Class II Z-1489-2026

Favicon for changeflow.com FDA: Device Recalls Class II
Detected March 29th, 2026
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Summary

Olympus Biopsy Valve Recall Class II Z-1489-2026

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Source document (simplified)

Olympus Corporation of the Americas

Device Recalls (Class II)

← All Device Recalls (Class II) Class II Z-1489-2026 · 20260311 · Ongoing

Product

Olympus Single Use Biopsy Valve. Model/Catalog Number: MAJ-1218. 20 units per box. The MAJ-1218 has been designed to be attached to the instrument channel port of compatible endoscopes to preven...

Reason for Recall

Potential for rubber fragment detachment during use.

Distribution

US Nationwide distribution.

Source: openFDA Enforcement API

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Source

Favicon for changeflow.com
FDA: Device Recalls Class II changeflow.com/changebridge/fda-enforcement/device-class-ii
Healthcare
Analysis generated by AI. Source diff and links are from the original.

Classification

Agency
FDA
Instrument
Notice

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