Medical Device Recalls
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1 result found
510(K) Number: K881261 |
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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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Plastic bottle containing 10.5 mL of IgG Conjugate Product Usage: Product is a used as a counter... | 3 | 06/05/2013 | Bion Enterprises Ltd |
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