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U.S. Department of Health and Human Services

Medical Device Recalls
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Related Medical Device Recalls
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Product Description
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FDA Recall
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Z-1000-2023 - AXIOM Luminos TF, AXIOM Iconos R100, AXIOM Iconos R200 and AXIOM Luminos dRF 2 01/20/2023 FEI # 2240869
Siemens Medical Solutions USA, Inc
Z-1002-2023 - Luminos Agile Max, Luminos dRF Max, and LUMINOS Lotus Max 2 01/20/2023 FEI # 2240869
Siemens Medical Solutions USA, Inc
Z-1001-2023 - AXIOM Luminos Agile 2 01/20/2023 FEI # 2240869
Siemens Medical Solutions USA, Inc
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