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Philips Integris Allura
No active recall
Manufacturer: Philips · FDA product code: IZI · Category: System, X-Ray, Angiographic
Severity Snapshot
36 total reports2001-04 – 2013-05 date range0% physician / facility reported100% manufacturer reported4 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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