Medical Device Recalls
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1 to 2 of 2 Results
510(K) Number: K130576 |
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Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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| Celsite Implantable Access Port System, model ST301. The Celsite Implantable Access Port Systems (C... | 2 | 08/13/2015 |
FEI # 3006332832 B. Braun Interventional Systems |
| Brand Name: CELSITE Product Name: CELSITE BABYPORT SET PUR 4,5F IV USA Model/Catalog Number: 54337... | 2 | 09/05/2025 |
FEI # 3002806713 B.Braun Medical S.A.S. |
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