Medical Device Recalls
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1 to 2 of 2 Results
510(K) Number: K053132 |
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Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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| Atellica CH Direct Bilirubin_2 assay In vitro Diagnostic for the determination of direct bilirubin ... | 2 | 03/20/2020 |
FEI # 2517506 Siemens Healthcare Diagnostics, Inc. |
| ADVIA Chemistry Direct Bilirubin_2 assay-SMN: 10316610 (20 mL) & 10341114 (70 mL) - Product Usage: ... | 2 | 03/20/2020 |
FEI # 2517506 Siemens Healthcare Diagnostics, Inc. |
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