Medical Device Recalls
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1 result found
510(K) Number: K043590 |
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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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Alaris® SE Pump (formerly Signature Edition® Infusion Pump); Model Numbers: 7000, 7100, 7101, 7130, ... | 1 | 09/19/2006 | Cardinal Health 303 Inc DBA Alaris Products |
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