Medical Device Recalls
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1 result found
510(K) Number: K951738 |
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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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| Catalog No. 8888160648; Umbilical Vessel Catheter 5 French triple lumen | 2 | 05/29/2025 | Cardinal Health 200, LLC |
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