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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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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| FreeStyle Precision H Blood Glucose and Ketone Monitoring System, UDI: 00093815711810 | 2 | 02/28/2020 | Abbott Diabetes Care, Inc. |
| Abbott Diabetes Care, Precision Point of Care Blood Glucose Test Strips; | 1 | 02/09/2011 | Abbott Diabetes Care, Inc. |
| Abbott Diabetes Care Precision Xceed Pro Blood Glucose Test Strips | 1 | 02/09/2011 | Abbott Diabetes Care, Inc. |
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