Medical Device Recalls
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1 result found
510(K) Number: K940867 |
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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 Continu-Flo Solution Set with Control-A-Flo Regulator, 89" (2.3 m), 2 Inject... | 2 | 01/11/2012 | Baxter Healthcare Corp. |
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