Medical Device Recalls
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1 result found
510(K) Number: K231587 |
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Results per Page |
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Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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| MAGNETOM Cima.X Upgrade. Model Number: 11689304. | 1 | 11/12/2025 | Siemens Medical Solutions USA, Inc |
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