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U.S. Department of Health and Human Services

Medical Device Recalls

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1 to 4 of 4 Results
510(K) Number: K022209
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Product Description
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FDA Recall
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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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