Medical Device Recalls
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11 to 12 of 12 Results
510(K) Number: K950419 |
Results per Page |
Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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Alaris Pump Module model 8100 | 2 | 06/19/2017 | CareFusion 303, Inc. |
Alaris Pump Module Model 8100 (formerly Medley Pump Module) Subsequent Product Code: FPA. The ... | 1 | 08/17/2012 | CareFusion 303, Inc. |
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