Medical Device Recalls
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1 result found
510(K) Number: K143548 |
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Results per Page |
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Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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| Owner's Booklets and Instructions for Use that are used with the following blood glucose measuring d... | 1 | 03/12/2026 |
FEI # 1000113657 Trividia Health, Inc. |
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