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U.S. Department of Health and Human Services

Medical Device Recalls
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31 to 40 of 63 Results
510(K) Number: K002507
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Product Description
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Arrow® Access Kit with Maximal Barrier Precautions for use with 5 Fr. Peripherally Inserted Central ... 2 06/06/2017 Arrow International Inc
Arrow® Access Kit with Maximal Barrier Precautions for use with 5 Fr. Peripherally Inserted Central ... 2 06/06/2017 Arrow International Inc
Arrow® VPS® Access Kit with Maximal Barrier Precautions for use with 4 Fr. Peripherally Inserted Cen... 2 06/06/2017 Arrow International Inc
Arrow® VPS® Access Kit with Maximal Barrier Precautions for use with 5 Fr. Peripherally Inserted Cen... 2 06/06/2017 Arrow International Inc
Arterial Catheterization Kit The Arrow® Arterial Catheterization device permits access to the perip... 2 06/06/2017 Arrow International Inc
Arterial Catheterization Kit with Maximal Barrier Precautions The Arrow® Arterial Catheterization... 2 06/06/2017 Arrow International Inc
Arterial Line Kit with Sharps Safety Features and Maximal Barrier Precautions The Arrow® Arterial C... 2 06/06/2017 Arrow International Inc
Femoral Arterial Line Catheterization Kit The Arrow® Arterial Catheterization device permits access... 2 06/06/2017 Arrow International Inc
Femoral Arterial Line Catheterization Kit The Arrow® Arterial Catheterization device permits access... 2 06/06/2017 Arrow International Inc
MAC Two-Lumen Central Venous Access kit with Integral Hemostasis Valve for use with 7 - 8 Fr. Cathet... 2 09/25/2010 Arrow International Inc
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