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Philips Integris
No active recall
Manufacturer: Philips · FDA product code: IZI · Category: System, X-Ray, Angiographic
Severity Snapshot
81 total reports1998-12 – 2014-09 date range6.3% physician / facility reported93.7% manufacturer reported7 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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