Medical Device Recalls
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1 to 2 of 2 Results
510(K) Number: K981995 |
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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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QuickDraw Venous Cannula, REF: QD22, UDI: 00690103182699; and REF: QD25, UDI: 00690103182705 | 2 | 01/10/2020 | Edwards Lifesciences, LLC |
QuickDraw Venous Cannula with Insertion Kit. ThruPort Systmes. Models QD22 (22 Fr) and QD25 (25 Fr).... | 2 | 06/13/2013 | Edwards Lifesciences, LLC |
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