Medical Device Recalls
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1 to 3 of 3 Results
510(K) Number: K193371 |
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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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FREESTYLE LIBRE 2 GLUCOSE MONITORING SYSTEM: Item number: 5658877 | 2 | 06/23/2021 | Cardinal Health Inc. |
FreeStyle Libre Reader, REF: 71951-01, 71952-01, 71953-01 a component of the FreeStyle Libre 2 Flash... | 1 | 04/06/2023 | Abbott Diabetes Care, Inc. |
FreeStyle Libre 2 Readers, REF: 71951-01 and 71953-01, used with FreeStyle Libre 2 System | 2 | 08/17/2023 | Abbott Diabetes Care, Inc. |
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