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U.S. Department of Health and Human Services

Medical Device Recalls
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1 to 9 of 9 Results
Related Medical Device Recalls
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Product Description
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Z-1486-2020 - Allura Exper FD Series. System codes 722003 722010 722022 722005 722011 722019 722001 722002 722006 722012 722008 722013 722020 722025 722015 722023 722038 889006 889016 889009 72... 2 03/13/2020 FEI # 1218950
Philips North America, LLC
Z-1487-2020 - Integris Allura 15 & 12, monoplane (system code 722043) and biplane (system code 722044) 2 03/13/2020 FEI # 1218950
Philips North America, LLC
Z-1488-2020 - Integris Allura 9, system codes 722018 722021 2 03/13/2020 FEI # 1218950
Philips North America, LLC
Z-1489-2020 - MultiDiagnost Eleva, System codes 722030 722016 722017 708032 708036 708034 708037 708038 2 03/13/2020 FEI # 1218950
Philips North America, LLC
Z-1494-2020 - Cardio Vascular-Allura Centron, system code 722400 2 03/13/2020 FEI # 1218950
Philips North America, LLC
Z-1491-2020 - Poly G Integris H5000, System code 72246 2 03/13/2020 FEI # 1218950
Philips North America, LLC
Z-1492-2020 - UroDiagnost Eleva, system code 708033 2 03/13/2020 FEI # 1218950
Philips North America, LLC
Z-1493-2020 - Allura CV20, system code 722031 2 03/13/2020 FEI # 1218950
Philips North America, LLC
Z-1490-2020 - OmniDiagnost Eleva System codes 708028 708027 2 03/13/2020 FEI # 1218950
Philips North America, LLC
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