Medical Device Recalls
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1 to 2 of 2 Results
510(K) Number: K061565 |
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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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Langston Dual Lumen Catheter. | 1 | 10/20/2020 | Vascular Solutions, Inc. |
Langston Dual Lumen Catheters, REF 5515, 7F, Sterile EO, Rx ONLY, 1 x Catheter and 5 x Catheter, Va... | 2 | 07/11/2011 | Vascular Solutions, Inc. |
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