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U.S. Department of Health and Human Services

Medical Device Recalls
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1 result found
510(K) Number: K201099
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Recall
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FDA Recall
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BD PhaSeal Injector Luer (N30C), REF: 515001 BD PhaSeal Injector Luer Lock (N35), REF: 515003 BD P... 2 08/27/2025 BD SWITZERLAND SARL
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