Medical Device Recalls
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11 to 20 of 29 Results
510(K) Number: K052202 |
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Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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| AXIOM Artis dFC, Model Number 7412807 | 2 | 07/22/2019 | Siemens Medical Solutions USA, Inc |
| AXIOM Artis dFA, Model Number 7555373 | 2 | 07/22/2019 | Siemens Medical Solutions USA, Inc |
| AXIOM Artis dBC, Model Number 7728392 | 2 | 07/22/2019 | Siemens Medical Solutions USA, Inc |
| AXIOM Artis dBC, Model Number 5917054 | 2 | 07/22/2019 | Siemens Medical Solutions USA, Inc |
| AXIOM Artis dBA, Model Number 7555357 | 2 | 07/22/2019 | Siemens Medical Solutions USA, Inc |
| AXIOM Artis and AXIOM Artis zee modular angiographic systems Product Usage: Angiographic x-ray sy... | 2 | 01/27/2012 | Siemens Medical Solutions USA, Inc |
| AXIOM Artis TC, Model Number 7728350 | 2 | 07/22/2019 | Siemens Medical Solutions USA, Inc |
| AXIOM Artis TA, Model Number 7007755 | 2 | 07/22/2019 | Siemens Medical Solutions USA, Inc |
| AXIOM Artis System dTC using software version VB31D with 30x40 cm2 flat detectors. ®AXIOM Artis i... | 2 | 12/09/2008 | Siemens Medical Solutions USA, Inc |
| AXIOM Artis System dTA using software version VB31D with 30x40 cm2 flat detectors. ®AXIOM Artis i... | 2 | 12/09/2008 | Siemens Medical Solutions USA, Inc |
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