Medical Device Recalls
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1 to 3 of 3 Results
510(K) Number: K040814 |
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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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Precision Xtra Blood Glucose & Ketone Monitoring System, UDI: 00093815715023, 00093815988144 | 2 | 02/28/2020 | Abbott Diabetes Care, Inc. |
Blood glucose meter, marketed with multiple brand names including: Precision Xtra New and Improved m... | 2 | 02/14/2008 | Abbott Diabetes Care, Inc. |
Precision Xtra Blood Glucose monitoring system. Individual test meter and test strip kit. | 3 | 06/07/2007 | Abbott Diabetes Care, Inc. |
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