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U.S. Department of Health and Human Services

Medical Device Recalls

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1 to 10 of 13 Results
510(K) Number: K190578
 
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Product Description
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FDA Recall
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SOMATOM Confidence -Computed tomography systems Model 10590100 2 01/10/2022 Siemens Medical Solutions USA, Inc
SOMATOM Definition AS-Computed tomography system Model 8098027 2 01/10/2022 Siemens Medical Solutions USA, Inc
SOMATOM Edge Plus-Computed tomography system Model 1026700 2 01/10/2022 Siemens Medical Solutions USA, Inc
SOMATOM Definition Edge -Computed tomography system Model 10590000 2 01/10/2022 Siemens Medical Solutions USA, Inc
SOMATOM Confidence with software syngo.CT VB20 Model #10590100 2 11/24/2021 Siemens Medical Solutions USA, Inc
SOMATOM Edge Plus with software syngo.CT VB20 Model #10267000 2 11/24/2021 Siemens Medical Solutions USA, Inc
SOMATOM Definition Flash with software syngo.CT VB20 Model #10430603 2 11/24/2021 Siemens Medical Solutions USA, Inc
SOMATOM Definition Edge with software syngo.CT VB20 Model #10590000 2 11/24/2021 Siemens Medical Solutions USA, Inc
SOMATOM Definition AS with software syngo.CT VB20 Model #8098027 2 11/24/2021 Siemens Medical Solutions USA, Inc
SOMATOM Force with software syngo.CT VB20 Model #10742326 2 11/24/2021 Siemens Medical Solutions USA, Inc
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