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-2665-2023 - therascreen ®KRAS RGQ PCR Kit (24)-IVD qualitative PCR assay used on the Rotor-Gene Q MDx instrument for the detection of seven somatic mutations in the human KRAS oncogene REF 870021 (US IVD) | 2 | 09/29/2023 |
FEI # 3004013603 Qiagen GmbH |
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