Medical Device Recalls
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1 result found
510(K) Number: K894827 |
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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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AUTOMIX 3+3 Compounder System, product 2M8286 (115V) and 2M8286K (230V), automated nutrition compoun... | 2 | 02/22/2011 | Baxter Healthcare Corp. |
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