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Stryker Emboguard 87
No active recall
Manufacturer: Stryker · FDA product code: QJP · Category: Catheter, Percutaneous, Neurovasculature
Severity Snapshot
56 total reports2022-05 – 2024-11 date range94.6% physician / facility reported5.4% 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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