NeuroMAUDE
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Stryker Vertecem V+ Cement

No active recall

Manufacturer: Stryker  · FDA product code: NDN  · Category: Cement, Bone, Vertebroplasty

Severity Snapshot

671 total reports2011-042026-03 date range68.3% physician / facility reported31.7% manufacturer reported2 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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