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U.S. Department of Health and Human Services

Medical Device Recalls

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1 to 10 of 19 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-1076-2025 - Allura CV20 System Code: 722031 2 02/04/2025 PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.
Z-1077-2025 - Allura Xper FD10 Catalog (1) 722003 (2) 722010 (3)722026 2 02/04/2025 PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.
Z-1079-2025 - Allura Xper FD10C System Code: (1) 722001 2 02/04/2025 PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.
Z-1085-2025 - Allura Xper FD20/20 System Code: (1) 722038 2 02/04/2025 PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.
Z-1078-2025 - AlluraXper FD10/10 System Code: (1) 722005 (2) 722011 (3) 722027 2 02/04/2025 PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.
Z-1080-2025 - AlluraXper FD20 System Code: (1) 722006 (2) 722012 (3) 722028 2 02/04/2025 PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.
Z-1081-2025 - AlluraXper FD20 Biplane System Code: (1) 722008 (2) 722013 2 02/04/2025 PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.
Z-1082-2025 - AlluraXper FD20 Biplane OR Table System Code: (1) 722020 (2) 722025 2 02/04/2025 PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.
Z-1083-2025 - AlluraXper FD20 OR Table System Code: (1) 722023 (2) 722035 2 02/04/2025 PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.
Z-1084-2025 - AlluraXperFD20/10 System Code: (1) 722029 2 02/04/2025 PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.
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