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U.S. Department of Health and Human Services

Medical Device Recalls
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1 to 10 of 10 Results
Related Medical Device Recalls Recall Date to: 08/02/2014
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Product Description
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Recall
Class
Sort by Recall Class [0-9]
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FDA Recall
Posting Date
Sort by Date Classified [0-9]
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Recalling Firm
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Z-0352-2009 - OminDiagnost Eleva 2 09/24/2009 Philips Medical Systems North America Co. Phillips
Z-0351-2009 - MultiDiagnost Eleva 2 09/24/2009 Philips Medical Systems North America Co. Phillips
Z-0347-2009 - Integris XPER FD10 F/C 2 09/24/2009 Philips Medical Systems North America Co. Phillips
Z-0345-2009 - Integris H5000F 2 09/24/2009 Philips Medical Systems North America Co. Phillips
Z-0346-2009 - Integris BH5000 2 09/24/2009 Philips Medical Systems North America Co. Phillips
Z-0350-2009 - Integris Allura Flat Detector 9C 2 09/24/2009 Philips Medical Systems North America Co. Phillips
Z-0353-2009 - EasyDiagnost Eleva x-ray systems 2 09/24/2009 Philips Medical Systems North America Co. Phillips
Z-0348-2009 - Allura XPER FD20/10 2 09/24/2009 Philips Medical Systems North America Co. Phillips
Z-0349-2009 - Allura XPER FD20 2 09/24/2009 Philips Medical Systems North America Co. Phillips
Z-0344-2009 - Allura XPER 10/10 2 09/24/2009 Philips Medical Systems North America Co. Phillips
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