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U.S. Department of Health and Human Services

Medical Device Recalls
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11 to 20 of 22 Results
510(K) Number: K830755
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Product Description
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FDA Recall
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150ML Burette IV Set with SmartSite(TM) Y-Injection Site, 2-Gang Standard Bore Stopcocks and T-Conne... 1 03/30/2010 Arrow International Inc
8" Microbore Extension with Detachable SmartSite(TM) HEP-Lock and Retractable Spinning Luerlock. DEH... 1 03/30/2010 Arrow International Inc
IV Set with Two SmartSite(TM) Y-Injection Sites, Stopcock and 3-Gang Pressure Activated Manifold Val... 1 03/30/2010 Arrow International Inc
8" Extension Set with SmartSite(TM) HEP-Lock and Rotating Luer Lock. SmartSite(TM) is a trademark of... 1 03/30/2010 Arrow International Inc
10 Drop IV Sets, with 3 Pre-Pierced Y-Injection Sites and 3-Gang Pressure Activated Manifold Valve. ... 1 03/30/2010 Arrow International Inc
Y-Type Positive Pressure Pump Set with 2-Gang 4-Way Stopcock and Detachable 4-Way Stopcock. An In... 1 03/30/2010 Arrow International Inc
7" Non-Kink Extension Set with Rotating Luer-Lock Connector. An Intravenous Administration Tubing... 1 03/30/2010 Arrow International Inc
Positive Pressure Blood Pumps, with Pre-Pierced Y-Injection Site; with Three SmartSite(TM)Injection ... 1 03/30/2010 Arrow International Inc
Y Type Blood Pump Sets, with 2 Vented Spikes and Double "Hi-Flo" Stopcock; with Luer Activated Y-Inj... 1 03/30/2010 Arrow International Inc
4-Way "Hi-Flo" Extension Set with Two SmartSite(TM) Y-Injection Sites and Rotating Luer Lock SmartSi... 1 03/30/2010 Arrow International Inc
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