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U.S. Department of Health and Human Services

Medical Device Recalls

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510(K) Number: K120836
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FDA Recall
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0.9% Sodium Chloride Injection, USP, 10mL in 12mL., Single use, Rx only, Sterile Solution. 2 08/27/2015 MRP, LLC dba AMUSA
T/S2 0.9% Sodium Chloride Injection, USP, AMUSA Sterile Field Flush Syringe, 10 mL in 12 mL Single U... 2 06/15/2015 MRP, LLC dba AMUSA
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