Medical Device Recalls
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1 to 3 of 3 Results
510(K) Number: K970485 |
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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 SmartSite Bag Access Device, REF: 2300E-0500; BD BAG ACCESS DEVICE CHECK VALVE SmartSite VALVE, R... | 2 | 09/13/2021 | CAREFUSION |
BD SmartSite Bag Access Device Needle-Free Valve, REF: 2300E; BD Bag access Device with 1 Check Valv... | 2 | 09/13/2021 | CAREFUSION |
SmartSite Add-On Bag Access Device, Model No. 10013365 | 2 | 04/27/2017 | CareFusion 303, Inc. |
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