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U.S. Department of Health and Human Services

Medical Device Recalls
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1 to 3 of 3 Results
Related Medical Device Recalls Recall Date to: 07/31/2014
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Product Description
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Recall
Class
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FDA Recall
Posting Date
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Recalling Firm
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Z-0118-2012 - Philips Verardius Image Intensified X-ray Catalog Number: 718130 Product Usage: Fluoroscopic x-ray system, image-intensified Fluoroscopic x-ray system. 2 10/27/2011 Philips Healthcare Inc.
Z-0116-2012 - Philips BV Pulsera Fluoroscopic Image Intensified X-ray Catalog Number: 718095 Product Usage: Fluoroscopic x-ray system, image-intensified Fluoroscopic x-ray system. 2 10/27/2011 Philips Healthcare Inc.
Z-0117-2012 - Philips BV Endura Fluoroscopic Image Intensified X-ray Catalog Number: 718074 Product Usage: Fluoroscopic x-ray system, image-intensified Fluoroscopic x-ray system. 2 10/27/2011 Philips Healthcare Inc.
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