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U.S. Department of Health and Human Services

Medical Device Recalls
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1 to 10 of 18 Results
510(K) Number: K200917
 
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Wireless Footswtich used with the following Philips Allura Xper and Azurion Interventional Fluorosco... 2 01/10/2022 Philips North America Llc
Wireless Foot Switch distributed with Philips Allura Xper and Azurion Interventional Fluoroscopic X-... 2 08/30/2023 PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.
Philips StentBoost Live R2.0 application, when used with the Philips Azurion with software release ... 2 04/05/2022 Philips Healthcare
Philips Azurion systems with software releases 2.1(L1) and 2.1(L2) 2 11/24/2021 Philips Healthcare
Philips Azurion systems with monoplane fixed ceiling mounts: 722078 Azurion 7 M12 722079 Azurion 7... 2 12/15/2023 PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.
Philips Azurion system, Interventional fluoroscopic x-ray system. System Product Name - Model Num... 2 01/26/2024 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 Systems, specifically the Disk Bay of the PC compo... 2 02/16/2024 PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.
Philips Allura Xper, Allura Centron, Allura CV, Azurion, UNIQ Clarity, and MultiDiagnost-Eleva syste... 2 09/14/2023 PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.
Philips Allura systems with monoplane fixed ceiling mounts: 722001 Allura Xper FD10C 722003 Allur... 2 12/15/2023 PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.
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