Medical Device Recalls
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1 to 3 of 3 Results
510(K) Number: K130725 |
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Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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| Catalog No. 8888160325; Umbilical Vessel Catheter 2.5 French single lumen | 2 | 05/29/2025 |
FEI # 3001236905 Cardinal Health 200, LLC |
| Catalog No. 8888160333; Umbilical Vessel Catheter 3.5 French single lumen | 2 | 05/29/2025 |
FEI # 3001236905 Cardinal Health 200, LLC |
| Catalog No. 8888160341; Umbilical Vessel Catheter 5 French single lumen | 2 | 05/29/2025 |
FEI # 3001236905 Cardinal Health 200, LLC |
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