Medical Device Recalls
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1 result found
510(K) Number: K900802 |
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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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CD4 (SK3), FITC; Contains CD4 FITC with gelatin and 0.1% sodium Azide. Catalog number 340133 in... | 3 | 09/24/2015 | Becton, Dickinson and Company, BD Biosciences |
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