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U.S. Department of Health and Human Services

Medical Device Recalls

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1 to 9 of 9 Results
Related Medical Device Recalls Date Classified to: 10/20/2014
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Product Description
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Recall
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Recalling Firm
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Z-2488-2010 - MAC Two-Lumen Central Venous Access kit with Integral Hemostasis Valve for use with 7 - 8 Fr. Catheters 2 Sep-25-2010 Arrow International Inc
Z-2489-2010 - Two-Lumen Central Venous Catheterization kit with Blue FlexTip Catheter (Sharps Safety Features) 2 Sep-25-2010 Arrow International Inc
Z-2490-2010 - Multi-Lumen Central Venous Catheterization kit with Blue FlexTip Catheter (Sharps Safety Features) 2 Sep-25-2010 Arrow International Inc
Z-2491-2010 - Multi-Lumen Pressure Injectable Central Venous Catheterization kit with Blue FlexTip Catheter, ARROW g+ard Blue PLUS Catheter and Sharps Safety Features 2 Sep-25-2010 Arrow International Inc
Z-2496-2010 - Two-Lumen Central Venous Catheterization Kit with Blue FlexTip ARROWg+ard Blue Catheter 2 Sep-25-2010 Arrow International Inc
Z-2493-2010 - Two-Lumen Central Venous Catheterization kit with Blue FlexTip ARROW g+ard Blue PLUS Catheter, Sharps Safety Features, and Maximal Barrier Precautions 2 Sep-25-2010 Arrow International Inc
Z-2494-2010 - Arterial Catheterization Set 2 Sep-25-2010 Arrow International Inc
Z-2495-2010 - Femoral Artery Catheterization Set 2 Sep-25-2010 Arrow International Inc
Z-2492-2010 - Two-Lumen Central Venous Catheterization kit with Blue FlexTip Catheter, ARROW g+ard Blue Catheter 2 Sep-25-2010 Arrow International Inc
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