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U.S. Department of Health and Human Services

Medical Device Recalls
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1 to 10 of 22 Results
510(K) Number: K181830
 
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VesselNavigator application used with Philips Azurion (Azurion 7 Series) Software R1.2 and R2.0, and... 2 02/10/2020 Philips North America, LLC
Phillips Azurion 7 M20, Angiographic X-Ray System Code 722079 Image guidance in diagnostic, inter... 2 04/24/2020 Philips North America, LLC
Philips Azurion Systems with software versions R2.1.10 and R2.2.10. Includes the following label des... 2 01/14/2026 PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.
Philips Azurion System configured with a 1 Phase UPS. Azurion family (R1.x, R2.x). Labeled as the fo... 2 09/03/2025 PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.
Philips Azurion System with software versions: R2.2.O, R2.2.1, R2.2.3, R2.2.5 and R2.2.6. Models/M... 2 09/30/2024 PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.
Philips Azurion Interventional Fluoroscopic X-ray Systems, specifically the Disk Bay of the PC compo... 2 02/16/2024 PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.
Philips Azurion Interventional Fluoroscopic X-ray System with Azurion R2.2 with LUC configuration st... 2 01/10/2022 Philips North America Llc
Philips Azurion Interventional Fluoroscopic X-Ray System, Software version 2.1.x, Model numbers 7220... 2 11/09/2021 Philips North America Llc
Philips Azurion 7 M20 -XperGuide Software hosted in Interventional Workspot 1.5 when used with the ... 2 04/29/2020 Philips North America, LLC
Philips Allura (Model Numbers 722010, 722012, 722026, 722027, 722028, 722029, 722035) and Philips Az... 2 04/06/2022 Philips North America Llc
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