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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: K873213
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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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BardPort M.R.I. Implantable Port with Attachale 9.6 F Open-Ended Single-Lumen Venous Catheter, REF: ... 2 03/26/2020 Bard Peripheral Vascular Inc
BardPort M.R.I. Hard Base Implantable Port with Attachable 9.6 F Open-Ended Single-Lumen Venous Cath... 2 03/26/2020 Bard Peripheral Vascular Inc
BardPort M.R.I. Implanted Port with Attachable 6 Fr. ChronoFlex Open-Ended Single-Lumen Venous Cathe... 3 03/01/2012 Bard Access Systems
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