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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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Recall
Class
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FDA Recall
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Recalling Firm
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Z-1480-2023 - Luminos dRF Max (VE10, VF10, VF11) 2 05/23/2023 FEI # 2240869
Siemens Medical Solutions USA, Inc
Z-1479-2023 - Luminos Agile Max (VE10, VF10, VF11) 2 05/23/2023 FEI # 2240869
Siemens Medical Solutions USA, Inc
Z-1481-2023 - LUMINOS Lotus Max (VF11) 2 05/23/2023 FEI # 2240869
Siemens Medical Solutions USA, Inc
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