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U.S. Department of Health and Human Services

Medical Device Recalls
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1 to 10 of 40 Results
510(K) Number: K160618
 
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System, Nuclear Magnetic Resonance Imaging - Product Usage: is a whole body magnetic resonance scann... 2 10/20/2020 GE Healthcare, LLC
System, Nuclear Magnetic Resonance Imaging - Product Usage: is a whole body magnetic resonance scann... 2 10/20/2020 GE Healthcare, LLC
SIGNA Artist, with affected software versions: DV26.0, DV27.1, DV28.1, DV29.1, MR30.0, MR30.1; Nucl... 2 08/02/2024 GE Medical Systems, LLC
SIGNA Artist, Nuclear Magnetic Resonance Imaging System 2 07/12/2021 GE Healthcare, LLC
SIGNA Artist nuclear magnetic resonance imaging system 2 10/16/2021 GE Healthcare, LLC
SIGNA Architect, with affected software versions: DV26.0 to DV26.3, DV27.0 to DV27.3, DV28.0 to DV2... 2 08/02/2024 GE Medical Systems, LLC
SIGNA Architect, Nuclear Magnetic Resonance Imaging System 2 11/22/2024 GE Medical Systems, LLC
SIGNA Architect system Product Usage: The Signa Architect system is a whole body magnetic resona... 2 10/24/2018 GE Medical Systems, LLC
SIGNA Architect AIR, Nuclear Magnetic Resonance Imaging System 2 11/22/2024 GE Medical Systems, LLC
SIGNA Architect - Product Usage: is a whole body magnetic resonance scanner designed to support high... 2 07/12/2021 GE Healthcare, LLC
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