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U.S. Department of Health and Human Services

Medical Device Recalls
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21 to 26 of 26 Results
Related Medical Device Recalls
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Z-2479-2024 - SIGNA Prime, with affected software versions: MR30.1; Nuclear Magnetic Resonance Imaging System 2 08/02/2024 GE Medical Systems, LLC
Z-2480-2024 - SIGNA Victor, with affected software versions: MR30.1; Nuclear Magnetic Resonance Imaging System 2 08/02/2024 GE Medical Systems, LLC
Z-2481-2024 - SIGNA UHP, with affected software versions: RX28.0, MR30.1; Nuclear Magnetic Resonance Imaging System - research use only 2 08/02/2024 GE Medical Systems, LLC
Z-2482-2024 - Discovery MR950, with affected software versions: 7T23.0; Nuclear Magnetic Resonance Imaging System - research use only 2 08/02/2024 GE Medical Systems, LLC
Z-2483-2024 - SIGNA 7.0T, with affected software versions: 7T29.1, MR30.1; Nuclear Magnetic Resonance Imaging System 2 08/02/2024 GE Medical Systems, LLC
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 2 08/02/2024 GE Medical Systems, LLC
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