Medical Device Recalls
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31 to 32 of 32 Results
510(K) Number: K051087 |
Results per Page |
Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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Dimension Vista 1500 Intelligent Lab System running on software versions V.3.6.1 SP1 or V.3.6.2, De... | 2 | 06/01/2016 | Siemens Healthcare Diagnostics Inc. |
Dimension Vista 1500 In-vitro diagnostic device intended to duplicate manual analytical procedures s... | 2 | 12/02/2021 | Siemens Healthcare Diagnostics, Inc. |
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