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U.S. Department of Health and Human Services

Medical Device Recalls

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1 to 4 of 4 Results
Related Medical Device Recalls
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Product Description
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Class
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FDA Recall
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Z-3165-2024 - System Code Name: 722282 Azurion 7 M20 722281 Azurion 5 M20 722236 Azurion 7 B20 722235 Azurion 7 B12 722234 Azurion 7 M20 722233 Azurion 7 M12 722228 Azurion 5 M20 722227 Azurion 5 M12 722226 Azurion... 2 09/18/2024 PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.
Z-3168-2024 - System Name: 708038 MultiDiagnost Eleva with Flat Detector 708037 MultiDiagnost Eleva with Flat Detector 708036 MultiDiagnost Eleva 708034 MultiDiagnost Eleva with Flat Detector 708032 MultiDiagnost E... 2 09/18/2024 PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.
Z-3167-2024 - System Name: 722044 INTEGRIS Allura 15-12 (biplane) 722030 Integris CV Cesar-Powerpack-Visub-Nicol 722021 INTEGRIS Allura 9 (biplane) 722018 Integris Allura 9 722017 Integris H5000 F / Allura 9F 72201... 2 09/18/2024 PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.
Z-3166-2024 - System Name: 722059 Allura Xper FD20/15 OR Table 722058 Allura Xper FD20/15 722039 Allura Xper FD20/20 OR Table 722038 Allura Xper FD20/20 722035 Allura Xper FD20 OR Table 722029 Allura Xper FD20/10 7... 2 09/18/2024 PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.
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