Medical Device Recalls
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1 to 2 of 2 Results
510(K) Number: K031676 |
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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 Lineo Opticap Disconnect Cap, product codes R5C4599Q (English) and N5C4599Q (dual English/Fre... | 2 | 07/20/2004 | Baxter Healthcare Corp. |
Baxter HomeChoice Automated PD Set with Lineo Connector, 4-prong, product codes R5C4479Q (English) a... | 2 | 07/20/2004 | Baxter Healthcare Corp. |
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