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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-1894-2019 - Siemens Artis zee floor -Interventional Fluoroscopic X-Ray System Model Number: 10094135 2 06/28/2019 FEI # 2240869
Siemens Medical Solutions USA, Inc
Z-1895-2019 - Siemens Artis zee ceiling -Interventional Fluoroscopic X-Ray System Model Number: 10094137 2 06/28/2019 FEI # 2240869
Siemens Medical Solutions USA, Inc
Z-1896-2019 - Siemens Artis zee biplane-Interventional Fluoroscopic X-Ray System Model Number: 10094141 2 06/28/2019 FEI # 2240869
Siemens Medical Solutions USA, Inc
Z-1897-2019 - Siemens Artis zeego--Interventional Fluoroscopic X-Ray System Model Number: 10280959 2 06/28/2019 FEI # 2240869
Siemens Medical Solutions USA, Inc
Z-1898-2019 - Siemens Artis Q floor --Interventional Fluoroscopic X-Ray System Model Number: 10848280 2 06/28/2019 FEI # 2240869
Siemens Medical Solutions USA, Inc
Z-1905-2019 - Siemens Artis pheno-Interventional Fluoroscopic X-Ray System Model Number: 10849000 2 06/28/2019 FEI # 2240869
Siemens Medical Solutions USA, Inc
Z-1900-2019 - Siemens Artis Q biplane---Interventional Fluoroscopic X-Ray System Model Number: 10848282 2 06/28/2019 FEI # 2240869
Siemens Medical Solutions USA, Inc
Z-1901-2019 - Siemens Artis Q zeego ---Interventional Fluoroscopic X-Ray System Model Number: 10848283 2 06/28/2019 FEI # 2240869
Siemens Medical Solutions USA, Inc
Z-1902-2019 - Siemens Artis Q.zen floor----Interventional Fluoroscopic X-Ray System Model Number: 10848353 2 06/28/2019 FEI # 2240869
Siemens Medical Solutions USA, Inc
Z-1903-2019 - Siemens Artis Q.zen ceiling-Interventional Fluoroscopic X-Ray System Model Number: 10848354 2 06/28/2019 FEI # 2240869
Siemens Medical Solutions USA, Inc
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