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U.S. Department of Health and Human Services

Medical Device Recalls
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1 to 4 of 4 Results
510(K) Number: K011975
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Product Description
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FDA Recall
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Outlook 400ES Safety Infusion System, Model Number 621-400ES. For use with B. Braun Medical Inc. Ho... 1 01/10/2011 FEI # 1641965
B Braun Medical, Inc
Outlook ES Safety Infusion System, Model 621-100ES, 621-200ES, 621-300ES, and 621-400ES B. Braun ... 2 10/03/2011 FEI # 1641965
B Braun Medical, Inc
Outlook ES pump is intended for use with B. Braun Medical Inc. Horizon Pump IV Sets. Used to regulat... 1 10/18/2011 FEI # 1641965
B Braun Medical, Inc
Outlook ES pump is intended for use with B. Braun Medical Inc. Horizon Pump IV Sets. Used to regulat... 1 09/13/2013 FEI # 1641965
B Braun Medical, Inc.
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