Medical Device Recalls
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1 result found
510(K) Number: K944757 |
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Results per Page |
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Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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| 3mL Safety-Lok Syringe, Catalog Number 309606, UDI 30382903096061 | 2 | 07/22/2019 |
FEI # 2243072 Becton Dickinson & Company |
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