Medical Device Recalls
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1 to 2 of 2 Results
510(K) Number: K233537 |
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Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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| FreeStyle Libre 3 Plus Sensor REF 78769-01 UDI-DI code: 00357599843014 The FreeStyle Libre 3 Plus s... | 1 | 01/14/2026 | Abbott Diabetes Care, Inc. |
| FreeStyle Libre 3 Plus Sensor REF 78768-01 UDI-DI code: 00357599844011 The FreeStyle Libre 3 Plus s... | 1 | 01/14/2026 | Abbott Diabetes Care, Inc. |
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