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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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FDA Recall
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Z-0166-2007 - Allura Xper FD 20/10 x-ray, and fluoroscopy 2 11/14/2006 FEI # 1000524572
Philips Medical Systems North America Co. Phillips
Z-0165-2007 - Allura X-per FD 10/10 x-ray, and fluoroscopy 2 11/14/2006 FEI # 1000524572
Philips Medical Systems North America Co. Phillips
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