Medical Device Recalls
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1 result found
510(K) Number: K222472 |
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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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| One Step Sterile Lancet for Single Use (3 sizes): 06949517008861 30g 06949517008854 28g 06949... | 3 | 10/21/2025 | Home Health US, Incorporated |
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