Medical Device Recalls
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1 result found
PMA Number: P050040 |
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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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SPOT-Light" HER2 CISH® Kit, catalog #84-0150, 20 tests/kit, labeled in part ***Invitrogen Corporatio... | 2 | 01/11/2012 | Life Technologies Corporation |
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