Medical Device Recalls
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1 result found
510(K) Number: K221032 |
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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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| Vascu-Guard Peripheral Vascular Patch (US), Product Codes: a) VG0108: 0.8 X 8 CM US, TS; b) VG01... | 2 | 01/05/2024 |
FEI # 1417572 Baxter Healthcare Corporation |
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