Medical Device Recalls
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1 to 3 of 3 Results
510(K) Number: K121434 |
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Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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| MAGNETOM Verio Dot. Model Number: 10684333. | 1 | 09/30/2025 |
FEI # 2240869 Siemens Medical Solutions USA, Inc |
| MAGNETOM Verio Dot Upgrade. Model Number: 10684334. | 1 | 09/30/2025 |
FEI # 2240869 Siemens Medical Solutions USA, Inc |
| MAGNETOM systems Aera/Skyra/Avanto/Verio with software syngo MR D13A ; indicated for use as magneti... | 2 | 03/20/2015 |
FEI # 2240869 Siemens Medical Solutions USA, Inc |
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