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U.S. Department of Health and Human Services

Medical Device Recalls
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510(K) Number: K163715
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Philips Azurion Rystem, Model Numbers: 722063, 722064, 722067, 722068, 722078, 722079, 722221, 722... 2 08/10/2026 FEI # 3042175844
PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.
Philips Allura System configured with a 1 Phase UPS. Allura family (R1.x, R2.x). Labeled as the ... 2 09/03/2025 FEI # 3002807880
PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.
Azurion 7 M20. Fluoroscopic X-Ray System. 2 07/18/2025 FEI # 3002807880
PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.
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