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U.S. Department of Health and Human Services

Medical Device Recalls

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1 to 10 of 12 Results
Related Medical Device Recalls
 
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Product Description
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Class
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FDA Recall
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Z-2303-2018 - Artis Q biplane, Material no. 10848282, for angiography and whole body radiographic/fluoroscopic procedures. 2 06/27/2018 Siemens Medical Solutions USA, Inc
Z-2304-2018 - Artis Q ceiling, Material no. 10848281, for angiography and whole body radiographic/fluoroscopic procedures. 2 06/27/2018 Siemens Medical Solutions USA, Inc
Z-2305-2018 - Artis Q.zen biplane, Material no. 10848355, for angiography and whole body radiographic/fluoroscopic procedures. 2 06/27/2018 Siemens Medical Solutions USA, Inc
Z-2306-2018 - Artis Q.zeego, Material no. 10848283, for angiography and whole body radiographic/fluoroscopic procedures. 2 06/27/2018 Siemens Medical Solutions USA, Inc
Z-2307-2018 - Artis Q.zen floor, Material no. 10848353, for angiography and whole body radiographic/fluoroscopic procedures. 2 06/27/2018 Siemens Medical Solutions USA, Inc
Z-2314-2018 - Artis zeego, Material no. 10280959 , for angiography and whole body radiographic/fluoroscopic procedures. 2 06/27/2018 Siemens Medical Solutions USA, Inc
Z-2309-2018 - Artis zee biplane MN, Material no. 10094143, for angiography and whole body radiographic/fluoroscopic procedures. 2 06/27/2018 Siemens Medical Solutions USA, Inc
Z-2310-2018 - Artis zee ceiling, Material no. 10094137, for angiography and whole body radiographic/fluoroscopic procedures. 2 06/27/2018 Siemens Medical Solutions USA, Inc
Z-2311-2018 - Artis zee floor, Material no. 10094135, for angiography and whole body radiographic/fluoroscopic procedures. 2 06/27/2018 Siemens Medical Solutions USA, Inc
Z-2312-2018 - Artis zee floor MN, Material no. 10094142, for angiography and whole body radiographic/fluoroscopic procedures. 2 06/27/2018 Siemens Medical Solutions USA, Inc
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