Medical Device Recalls
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1 result found
510(K) Number: K082725 |
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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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Vasoshield Syringe Packs, Model VH-5001 | 2 | 01/19/2023 | Maquet Cardiovascular, LLC |
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