Medical Device Recalls
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1 result found
510(K) Number: K812973 |
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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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Cournand Modified 2-PC 19G, 5.4cm or (Guidewire Introducer Needle) 20 units per case The Stryker G... | 2 | 12/14/2015 | Stryker Instruments Div. of Stryker Corporation |
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