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Product Description
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Recall Class
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FDA Recall Posting Date
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Recalling Firm
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Z-2469-2024 - SIGNA Artist, with affected software versions: DV26.0, DV27.1, DV28.1, DV29.1, MR30.0, MR30.1; Nuclear Magnetic Resonance Imaging System
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2
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08/02/2024
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GE Medical Systems, LLC
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Z-2470-2024 - SIGNA Voyager, with affected software versions: PX26.0 to PX26.6, VX28.0, VX29.1, VX29.2, MR30.0, MR30.1; Nuclear Magnetic Resonance Imaging System
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2
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08/02/2024
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GE Medical Systems, LLC
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Z-2471-2024 - 1.5T SIGNA HDxt Family, with affected software versions: HD16.0_V03 to HD16.4, HD23.0_V03, HD28.0, HD29.1, MR30.0, MR30.1; Nuclear Magnetic Resonance Imaging System
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2
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08/02/2024
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GE Medical Systems, LLC
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Z-2472-2024 - SIGNA Creator, with affected software versions: HD16.0_V03 to HD16.4, HD23.0_V03, HD28.0, HD29.1, MR30.0, MR30.1; Nuclear Magnetic Resonance Imaging System
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2
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08/02/2024
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GE Medical Systems, LLC
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Z-2473-2024 - SIGNA Explorer, with affected software versions: SV25.5, SV25.6, SV29.2, MR30.0, MR30.1; Nuclear Magnetic Resonance Imaging System
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2
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08/02/2024
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GE Medical Systems, LLC
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Z-2474-2024 - SIGNA MR380, with affected software versions: SV25.5, SV25.6; Nuclear Magnetic Resonance Imaging System
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2
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08/02/2024
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GE Medical Systems, LLC
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Z-2475-2024 - SIGNA MR355, with affected software versions: SV25.5, SV25.6; Nuclear Magnetic Resonance Imaging System
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2
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08/02/2024
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GE Medical Systems, LLC
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Z-2476-2024 - SIGNA MR360, with affected software versions: SV25.5, SV25.6; Nuclear Magnetic Resonance Imaging System
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2
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08/02/2024
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GE Medical Systems, LLC
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Z-2477-2024 - Brivo MR355, with affected software versions: SV20.3, SV23.3, MR30.0, MR30.1; Nuclear Magnetic Resonance Imaging System
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2
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08/02/2024
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GE Medical Systems, LLC
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Z-2478-2024 - Optima MR360, with affected software versions: SV20.3, SV23.3, MR30.0, MR30.1; Nuclear Magnetic Resonance Imaging System
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2
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08/02/2024
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GE Medical Systems, LLC
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