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Olympus Hydra
No active recall
Manufacturer: Olympus · FDA product code: FEQ · Category: Pump, Air, Non-Manual, For Endoscope
Severity Snapshot
24 total reports2018-04 – 2025-11 date range29.2% physician / facility reported70.8% manufacturer reported1 SKU variants
Reporting Trend
Annual Reporting Volume
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Note: the 2018 Voluntary Malfunction Summary Reporting expansion means volume increases may reflect surveillance changes, not increased device risk.
Reported Events
Submitted to FDA MAUDE by physicians, hospitals, manufacturers, and patients.
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