Medical Device Recalls
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1 to 4 of 4 Results
510(K) Number: K022209 |
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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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BD Alaris Pump infusion sets (Product Name, Catalog #) BD AlarisTM Pump Infusion Set Vented syrin... | 2 | 11/17/2023 | Becton Dickinson & Company |
BD Extension Sets (Product Name, Catalog #) BD SmartSite Filter Extension Set PE lined Standard b... | 2 | 11/17/2023 | Becton Dickinson & Company |
BD gravity sets (Product Name, Catalog #) 32-IN GRAV SET W/0.2 MICRON FILTER BAG ACCESS PORT SS V... | 2 | 11/17/2023 | Becton Dickinson & Company |
Alaris® SE Pump (formerly Signature Edition® Infusion Pump); Model Numbers: 7000, 7100, 7101, 7130, ... | 1 | 09/19/2006 | Cardinal Health 303 Inc DBA Alaris Products |
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