Medical Device Recalls
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1 to 6 of 6 Results
510(K) Number: K022209 |
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Results per Page |
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Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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| BD Alaris Pump Infusion Sets for the following reference numbers: C24101E, Amber Tubing, 15 Micron... | 1 | 10/08/2025 |
FEI # 2016493 CareFusion 303, Inc. |
| BD Alaris Pump Infusion Sets REF: 10013186, BD Alaris Pump Infusion Set, Back Check Valve, 3 Smar... | 1 | 08/06/2025 |
FEI # 2016493 CareFusion 303, Inc. |
| Alaris Pump Infusion Set Low Sorbing Tubing (PE Lined) Back Check Valve 2 SmartSite Y Sites REF 100... | 2 | 05/31/2024 |
FEI # 3012798826 BD SWITZERLAND SARL |
| BD Extension Sets (Product Name, Catalog #) BD SmartSite Filter Extension Set PE lined Standard b... | 2 | 11/17/2023 |
FEI # 2243072 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 |
FEI # 2243072 Becton Dickinson & Company |
| BD Alaris Pump infusion sets (Product Name, Catalog #) BD AlarisTM Pump Infusion Set Vented syrin... | 2 | 11/17/2023 |
FEI # 2243072 Becton Dickinson & Company |
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