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U.S. Department of Health and Human Services

Medical Device Recalls
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1 to 6 of 6 Results
510(K) Number: K063377
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Product Description
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Recall
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FDA Recall
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PowerPort isp M.R.I. Implantable Port with Attachable 8F Polyurethane Open-Ended Single-Lumen Venous... 2 11/27/2019 FEI # 2020394
Bard Peripheral Vascular Inc
POWERPORT ClearVUE isp with Smooth Septum, 8F ChronoFlex, Polyurethane Catheter, REF 1668362 2 05/09/2018 FEI # 2020394
Bard Peripheral Vascular Inc
POWERPORT ClearVUE isp with Smooth Septum, 8F ChronoFlex, Polyurethane Catheter, REF 5668362 2 05/09/2018 FEI # 2020394
Bard Peripheral Vascular Inc
POWERPORT ClearVUE isp Implantable Port With Smooth Septum and Attachable 8F Polyurethane Open-Ended... 2 05/09/2018 FEI # 2020394
Bard Peripheral Vascular Inc
POWERPORT(R) ClearVUE(R) isp with Smooth Septum, 6F ChronoFlex(TM), Polyurethane Catheter, REF 16663... 2 05/09/2018 FEI # 2020394
Bard Peripheral Vascular Inc
POWERPORT ClearVUE isp with Smooth Septum, 6F ChronoFlex, Polyurethane Catheter, REF 5666362 2 05/09/2018 FEI # 2020394
Bard Peripheral Vascular Inc
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