Medical Device Recalls
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1 result found
510(K) Number: K840261 |
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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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| ADVIA® 120/2120/2120i SETpoint Calibrator | 2 | 07/03/2025 | Siemens Healthcare Diagnostics, Inc. |
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