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 manufactured between November 2011 and March 2012; Alaris Pump Modul... | 2 | 10/19/2017 | CareFusion 303, Inc. |
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