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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: K070984
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Product Description
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FDA Recall
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Abbott Diabetes Care Precision Xceed Pro Blood Glucose Test Strips 1 02/09/2011 Abbott Diabetes Care, Inc.
Abbott Diabetes Care, Precision Point of Care Blood Glucose Test Strips; 1 02/09/2011 Abbott Diabetes Care, Inc.
FreeStyle Precision H Blood Glucose and Ketone Monitoring System, UDI: 00093815711810 2 02/28/2020 Abbott Diabetes Care, Inc.
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