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U.S. Department of Health and Human Services

Medical Device Recalls
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1 to 10 of 15 Results
Related Medical Device Recalls Recall Date to: 09/02/2015
 
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Product Description
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Recall
Class
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FDA Recall
Posting Date
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Recalling Firm
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Z-1489-2009 - Arrow 4way Hi-Flo Stopcock with male luer lock, latex free used in various IV kits. 2 06/24/2009 Arrow International Inc
Z-1503-2009 - Arrow Peripherally Inserted Central Catheter 2 06/24/2009 Arrow International Inc
Z-1491-2009 - Arrow Super Arrow-Flex Percutaneous Sheath Introducers 2 06/24/2009 Arrow International Inc
Z-1492-2009 - Arrow ARROWg+ard Super Arrow-Flex Percutaneous Sheath Introducers 2 06/24/2009 Arrow International Inc
Z-1493-2009 - Arrow Percutaneous Sheath Introducers 2 06/24/2009 Arrow International Inc
Z-1494-2009 - Arrow Single Lumen CVCs (Central Venous Catheters) 2 06/24/2009 Arrow International Inc
Z-1495-2009 - Arrow Multi-Lumen CVC w/ BlueFlex Tip (Central Venous Catheter) 2 06/24/2009 Arrow International Inc
Z-1496-2009 - Arrow Two-Lumen Central Venous Access (MAC) 2 06/24/2009 Arrow International Inc
Z-1497-2009 - Arrow ARROWg+ard Quad-Lumen CVCs (Central Venous Catheters) 2 06/24/2009 Arrow International Inc
Z-1498-2009 - Arrow ARROWg+ard Blue Plus Multi-Lumen CVCs (Central Venous Catheters) 2 06/24/2009 Arrow International Inc
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