Medical Device Recalls
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11 to 12 of 12 Results
510(K) Number: K950419 |
Results per Page |
Product Description
|
Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
|
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Alaris Pump Module, Model 8100. | 1 | 08/03/2009 | Cardinal Health 303 dba Cardinal Health |
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 |
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