Medical Device Recalls
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1 result found
510(K) Number: K970438 |
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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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Baxter Interlink System, Micro-Infusion Manifold; and Interlink Manifold. An Rx sterile device with... | 2 | 12/01/2010 | Baxter Healthcare Corp. |
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