Medical Device Recalls
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1 result found
510(K) Number: K081846 |
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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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GrebSet Micro-Introducer Kit, model 7941, Sterilized with Ethylene Oxide. Product Usage: The Gr... | 2 | 02/23/2017 | Vascular Solutions, Inc. |
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