Medical Device Recalls
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1 to 2 of 2 Results
510(K) Number: K132119 |
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Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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| MAGNETOM Prisma. Model Number: 10849582. | 1 | 09/30/2025 | Siemens Medical Solutions USA, Inc |
| MAGNETOM Prisma magnetic resonance diagnostic devices Model #10849582 | 2 | 08/22/2019 | Siemens Medical Solutions USA, Inc |
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