Medical Device Recalls
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1 to 2 of 2 Results
510(K) Number: K882302 |
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Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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| CareFusion SmartSite Gravity Blood Set Model 42082E. Used to administer blood and blood products t... | 2 | 02/15/2013 | Carefusion 303 Inc |
| 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 |
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