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U.S. Department of Health and Human Services

Medical Device Recalls
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Related Medical Device Recalls
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Product Description
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Z-0330-2008 - Allura Xper FD20/10, Release 1.2, Philips Medical Systems, Bothell, WA 98021 2 12/07/2007 FEI # 1000524572
Philips Medical Systems North America Co. Phillips
Z-0329-2008 - Allura Xper FD20 X-Ray System, Release 2.2, Philips Medical Systems, Bothell, WA 98021 2 12/07/2007 FEI # 1000524572
Philips Medical Systems North America Co. Phillips
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