Medical Device Recalls
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1 to 2 of 2 Results
510(K) Number: K050310 |
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Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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| BardPort Titanium Implantable Port with Attachable 9.6 F Open-Ended Single-Lumen Venous Catheter , R... | 2 | 03/26/2020 |
FEI # 2020394 Bard Peripheral Vascular Inc |
| BardPort Titanium Implanted Port. Bard Access Systems. Assembled in Mexico. A totally implantab... | 3 | 09/08/2011 |
FEI # 3006260740 Bard Access Systems |
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