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Air Oscillator
No active recall
FDA product code: HWE · Category: Instrument, Surgical, Orthopedic, Ac-Powered Motor And Accessory/Attachment
Severity Snapshot
661 total reports2013-05 – 2026-01 date range0.5% physician / facility reported99.5% manufacturer reported1 SKU variants
Failure & Consequence Profiles
Top Failure Modes
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Top Patient Outcomes
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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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