Medical Device Recalls
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1 result found
510(K) Number: K130394 |
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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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CADD®- Solis Ambulatory Infusion Pump, Model 2111 & 2112, Version 1.0, Version 2.0 and Version 3.0 &... | 2 | 06/18/2015 | Smiths Medical ASD, Inc. |
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