Medical Device Recalls
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1 to 2 of 2 Results
510(K) Number: K894842 |
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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 Infusion Pump administration sets labeled as: -Infusion Set Alaris Pump Module/Medley Pump ... | 2 | 11/04/2018 | CareFusion 303, Inc. |
Alaris Pump Infusion Set, Model Codes 10010453, 10010454, 10012144, 10015294, 10015414, 10933805, 11... | 1 | 07/11/2019 | Becton Dickinson & Company |
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