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U.S. Department of Health and Human Services

Medical Device Recalls

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1 to 6 of 6 Results
Related Medical Device Recalls
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Product Description
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FDA Recall
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Z-0442-2024 - ELEKTA LIMITED Precise Digital Accelerator, REF MRT 6001, MRT 6011; Medical Charged-Particle Radiation Therapy System Accelerator, Linear 2 12/01/2023 Elekta, Inc.
Z-0443-2024 - ELEKTA LIMITED Elekta Synergy, REF MRT 8501, MRT 8511; Medical Charged-Particle Radiation Therapy System Accelerator, Linear 2 12/01/2023 Elekta, Inc.
Z-0447-2024 - ELEKTA AXESSE, REF XRT 2181, XRT 27891; Medical Charged-Particle Radiation Therapy System Accelerator, Linear 2 12/01/2023 Elekta, Inc.
Z-0445-2024 - ELEKTA LIMITED Versa HD, REF XRT 2121, 2131; Medical Charged-Particle Radiation Therapy System Accelerator, Linear 2 12/01/2023 Elekta, Inc.
Z-0446-2024 - ELEKTA LIMITED Elekta Infinity, REF XRT 0511, XRT 0521, XRT 0531, XRT 0541; Medical Charged-Particle Radiation Therapy System Accelerator, Linear 2 12/01/2023 Elekta, Inc.
Z-0444-2024 - ELEKTA LIMITED Elekta Synergy Platform, REF MRT 8501, MRT 8511; Medical Charged-Particle Radiation Therapy System Accelerator, Linear 2 12/01/2023 Elekta, Inc.
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