Medical Device Recalls
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1 to 2 of 2 Results
510(K) Number: K081975 |
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Results per Page |
Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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Optium EZ Blood Glucose Monitoring System, UDI: 00093815710653 | 2 | 02/28/2020 | Abbott Diabetes Care, Inc. |
Abbott Diabetes Care Optium EZ Blood Glucose Test Strips; | 1 | 02/09/2011 | Abbott Diabetes Care, Inc. |
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