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U.S. Department of Health and Human Services

Medical Device Recalls
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1 to 6 of 6 Results
Related Medical Device Recalls
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Z-0366-2007 - Philips Integris Allura x-ray systems angiographic - Allura 9 F/C (floor and ceiling models). A mono-plane analog Allura with a 9' Image Intensifier 2 01/25/2007 FEI # 1000524572
Philips Medical Systems North America Co. Phillips
Z-0367-2007 - Allura Mono X-Ray System, angiographic - monoplane, analog Allura with a 12' and 15' Image Intensifier 2 01/25/2007 FEI # 1000524572
Philips Medical Systems North America Co. Phillips
Z-0371-2007 - FD 20/10 X-Ray System, Angiograph, biplane, digital Allura FD, 10' and 20' detectors 2 01/25/2007 FEI # 1000524572
Philips Medical Systems North America Co. Phillips
Z-0369-2007 - Allura FD20 x-ray system, angiograph, monoplane, digital Allura FD with a 20' detector FD 2 01/25/2007 FEI # 1000524572
Philips Medical Systems North America Co. Phillips
Z-0370-2007 - FD 10/10 X-Ray System, Angiograph, bi-plane digital Allura FD, 10' detector 2 01/25/2007 FEI # 1000524572
Philips Medical Systems North America Co. Phillips
Z-0368-2007 - Allura FD 10 FC, X-Ray System, angiographic - a monoplane, digital Allura FD (flat detector) with a 10' Image Intensifier (II). 2 01/25/2007 FEI # 1000524572
Philips Medical Systems North America Co. Phillips
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