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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-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-2480-2024 - SIGNA Victor, with affected software versions: 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-2481-2024 - SIGNA UHP, with affected software versions: RX28.0, MR30.1; Nuclear Magnetic Resonance Imaging System - research use only
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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-2479-2024 - SIGNA Prime, with affected software versions: 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-2462-2024 - SIGNA Premier, with affected software versions: RX27.0 to RX27.3, RX28.0, RX29.0 to RX29.2, 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-2460-2024 - SIGNA Pioneer, with affected software versions: PX25.0 to PX25.5, PX26.0, PX26.1, PX28.0 to PX28.4, PX29.0, PX29.1, 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-2466-2024 - SIGNA PET/MR, with affected software versions: MP24.0, MP26.0, MP26.1, MR30.0, MR30.1; Tomographic imager combining emission computed tomography with nuclear magnetic resonance
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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-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-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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