Medical Device Recalls
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1 result found
510(K) Number: K202145 |
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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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| Bigfoot Unity Diabetes Management System SW-300689-01 Bigfoot Inject v1 Pen Cap LCAP Firmware 1.3.0 ... | 2 | 06/20/2025 | BIGFOOT BIOMEDICAL |
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