Medical Device Recalls
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1 result found
PMA Number: P890064/S007 |
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Results per Page |
Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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Hybrid Capture 2 High-Risk HPV DNA Test, Catalog # 5101-1296 | 2 | 03/19/2003 | Digene Corp |
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