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Stryker Sagittal Saw
No active recall
Manufacturer: Stryker · FDA product code: KIJ · Category: Instrument, Surgical, Orthopedic, Dc-Powered Motor And Accessory/Attachment
Severity Snapshot
43 total reports2009-10 – 2025-11 date range2.6% physician / facility reported97.4% manufacturer reported2 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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