Medical Device Recalls
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1 to 3 of 3 Results
510(K) Number: K032233 |
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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 PCA Pump, Model 8120. The firm name on the label is CareFusion. The Alaris Syringe Pump m... | 2 | 01/08/2018 | CareFusion 303, Inc. |
Alaris System Inter-Unit Interface (IUI) Connectors. The Modules include the following: Alaris PC U... | 1 | 08/03/2009 | Cardinal Health 303 dba Cardinal Health |
Alaris Patient-Controlled Analgesia (PCA) Module (formerly Medley PCA Module) Model 8120 used with t... | 2 | 05/01/2009 | Cardinal Health 303 dba Cardinal Health |
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