Medical Device Recalls
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1 to 2 of 2 Results
510(K) Number: K010566 |
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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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Colleague Single Channel Volumetric Infusion Pumps, product code 2M8151and 2M8151R; Baxter Healthcar... | 2 | 12/22/2004 | Baxter Healthcare Corp. |
Colleague Single Channel Volumetric Infusion Pumps, product code 2M8151and 2M8151K (United Kingdom);... | 2 | 07/20/2004 | Baxter Healthcare Corp. |
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