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U.S. Department of Health and Human Services

Medical Device Recalls

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1 to 2 of 2 Results
Related Medical Device Recalls Recall Date to: 03/30/2015
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Product Description
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FDA Recall
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Z-1254-2009 - AXIOM Sireskop SD Model numbers 8890415 and 8890407. The product is intended for use as radiographic and fluoroscopic imaging device. 2 05/06/2009 Siemens Medical Solutions USA, Inc
Z-1253-2009 - AXIOM Sireskop SX Model numbers 3111676 and 3111668. The product is intended for use as radiographic and fluoroscopic imaging device. 2 05/06/2009 Siemens Medical Solutions USA, Inc
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