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U.S. Department of Health and Human Services

Medical Device Recalls
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Z-2205-2019 - Philips Azurion systems with software version R1.2 -Interventional Fluoroscopic X-ray system as follows: Azurion 3 M12, Azurion 3 M15, Azurion 7 B12, Azurion 7 B20, Azurion 7 M12, Azurion 7 M20 M... 2 08/06/2019 FEI # 1218950
Philips North America, LLC
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