Medical Device Recalls
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1 result found
510(K) Number: K121050 |
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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 0.9 Sodium Chloride Injection, USP 10 mL REF 306553. Intende... | 2 | 09/22/2014 | Becton Dickinson & Company |
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