Medical Device Recalls
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1 result found
510(K) Number: K911141 |
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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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| HEMOCUE INC F/GLUCOSE 201 ANALYZER (25/VL 4VL/BX) MICROCUVETTE. | 2 | 05/27/2025 | Mckesson Medical-Surgical Inc. Corporate Office |
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