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U.S. Department of Health and Human Services

Medical Device Recalls
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1 to 3 of 3 Results
510(K) Number: K050805
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Recall
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FDA Recall
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Pedi-Pak Pedi-Syringe Filter 30 mL Becton Dickinson Syringe Rx Only Genesis BPS, LLC The intended ... 2 09/18/2014 FEI # 1000527169
Genesis BPS, LLC.
Pedi-Pak Pedi-Syringe Filter 35 mL Monoject Syringe Rx Only Genesis BPS, LLC The intended use is t... 2 09/18/2014 FEI # 1000527169
Genesis BPS, LLC.
Pedi-Pak Pedi-Syringe Filter 60 mL Becton Dickinson/Monoject Syringe Rx Only Genesis BPS, LLC The ... 2 09/18/2014 FEI # 1000527169
Genesis BPS, LLC.
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