Medical Device Recalls
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1 to 2 of 2 Results
510(K) Number: K931550 |
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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 SE Burette Set 20 Drops 2 Injection Ports Vented/NonVented, REF: 72103E-0006 | 2 | 09/13/2021 | CAREFUSION |
SmartSite Low Sorbing Infusion Set, Model#72313E The SmartSite Low Sorbing Infusion Sets are used... | 2 | 09/26/2013 | CareFusion 303, Inc. |
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