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U.S. Department of Health and Human Services

Medical Device Recalls
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1 to 3 of 3 Results
510(K) Number: K073423
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Product Description
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Recall
Class
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FDA Recall
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Recalling Firm
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1.PowerPort Implantable Port With Attachable 9.6 F Open-Ended Single-Lumen Venous Catheter REF: 1709... 2 03/26/2020 FEI # 2020394
Bard Peripheral Vascular Inc
1. Power Port isp M.R.I. Implantable Port with Attachable 9.6 F Open-Ended Single-Lumen Venous Cathe... 2 03/26/2020 FEI # 2020394
Bard Peripheral Vascular Inc
1. PowerPort M.R.I. Implantable Port with Attachable 9.6 F Open-Ended Single-Lumen Venous Catheter w... 2 03/26/2020 FEI # 2020394
Bard Peripheral Vascular Inc
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