Medical Device Recalls
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1 result found
Related Medical Device Recalls |
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Product Description
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Recall
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FDA Recall
Posting Date |
Recalling Firm
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| Z-1544-2025 - GenetiSure Dx Labeling Kit, REF: K1201-64105, contains human reference DNA female aliquot, REF5190-7317. A required kit for the GenetiSure Dx Postnatal assay (K1201A). | 2 | 04/08/2025 |
FEI # 2916205 Agilent Technologies, Inc. |
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