Medical Device Recalls
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1 to 2 of 2 Results
510(K) Number: K141102 |
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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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Hospira MedNet Medication Management Suite software, version 6.1, List Numbers 16037-64-02 and 16037... | 2 | 09/13/2016 | Hospira Inc., A Pfizer Company |
ICU Mednet(TM) Medication Management Suite 6.1 and 6.21, Product Code/List Numbers: (a) 16037-64-01... | 2 | 12/06/2017 | ICU Medical Inc |
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