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Stryker 11G Ivas Access Cannula
No active recall
Manufacturer: Stryker · FDA product code: OAR · Category: Injector, Vertebroplasty (Does Not Contain Cement)
Severity Snapshot
55 total reports2015-03 – 2026-02 date range9.1% physician / facility reported90.9% 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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