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U.S. Department of Health and Human Services

Medical Device Recalls

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1 to 9 of 9 Results
Related Medical Device Recalls Recall Date to: 10/22/2014
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Product Description
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FDA Recall
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Z-0123-2009 - Axiom Artis dTC, Axiom Artis Modular Angiography X-Ray System, Model number 7413078. 2 11/25/2008 Siemens Medical Solutions USA, Inc
Z-0122-2009 - Axiom Artis dTA, Axiom Artis Modular Angiography X-Ray System, Model number 7008605. 2 11/25/2008 Siemens Medical Solutions USA, Inc
Z-0127-2009 - Axiom Artis dMP, Axiom Artis Modular Angiography X-Ray System, Model number 7555365. 2 11/25/2008 Siemens Medical Solutions USA, Inc
Z-0125-2009 - Axiom Artis dFC-M, Axiom Artis Modular Angiography X-Ray System, Model number 7727717. 2 11/25/2008 Siemens Medical Solutions USA, Inc
Z-0120-2009 - Axiom Artis dFC, Axiom Artis Modular Angiography X-Ray System, Model number 7412807. 2 11/25/2008 Siemens Medical Solutions USA, Inc
Z-0126-2009 - Axiom Artis dFA, Axiom Artis Modular Angiography X-Ray System, Model number 7555373. 2 11/25/2008 Siemens Medical Solutions USA, Inc
Z-0121-2009 - Axiom Artis dBC-M, Axiom Artis Modular Angiography X-Ray System, Model number 5917054. 2 11/25/2008 Siemens Medical Solutions USA, Inc
Z-0128-2009 - Axiom Artis dBC, Axiom Artis Modular Angiography X-Ray System, Model number 7728392. 2 11/25/2008 Siemens Medical Solutions USA, Inc
Z-0124-2009 - Axiom Artis dBA, Axiom Artis Modular Angiography X-Ray System, Model number 7555357. 2 11/25/2008 Siemens Medical Solutions USA, Inc
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