Medical Device Recalls
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1 result found
510(K) Number: K153481 |
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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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BD Posiflush SF Saline Flush Syringe (US Distributed Catalog 306553), UDI 50382903065535 | 2 | 05/21/2020 | Becton Dickinson & Company |
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