Medical Device Recalls
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1 result found
510(K) Number: K112082 |
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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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Vascular Solutions, GuideLiner V2 Catheter, Rx only, Sterile EO, Catalog Number 5571, 6F, Vascular S... | 2 | 05/24/2012 | Vascular Solutions, Inc. |
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