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U.S. Department of Health and Human Services

Medical Device Recalls
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1 to 5 of 5 Results
510(K) Number: K040172
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Product Description
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Recall
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FDA Recall
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Discovery LS, 2286327 LightSpeed 4.0 CT Scanner System - The LightSpeed 4.0 CT Scanner System is ... 2 03/04/2016 GE Medical Systems, LLC
Discovery ST, , 2339985 LightSpeed 4.0 CT Scanner System - The LightSpeed 4.0 CT Scanner System is ... 2 03/04/2016 GE Medical Systems, LLC
LightSpeed Plus (4-slice MDAS LightSpeed 4.0 CT Scanner System - The LightSpeed 4.0 CT Scanner Syst... 2 03/04/2016 GE Medical Systems, LLC
PET Discovery LS 2 09/21/2015 GE Healthcare
Lightspeed 16 CT 2 09/21/2015 GE Healthcare
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