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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: 08/22/2014
 
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Product Description
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Recall
Class
Sort by Recall Class [0-9]
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FDA Recall
Posting Date
Sort by Date Classified [0-9]
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Recalling Firm
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Z-1496-2009 - Arrow Two-Lumen Central Venous Access (MAC) 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-1494-2009 - Arrow Single Lumen CVCs (Central Venous Catheters) 2 06/24/2009 Arrow International Inc
Z-1503-2009 - Arrow Peripherally Inserted Central Catheter 2 06/24/2009 Arrow International Inc
Z-1501-2009 - Arrow Percutaneous Thrombolytic Device (PTD) for fistula and dialysis grafts 2 06/24/2009 Arrow International Inc
Z-1493-2009 - Arrow Percutaneous Sheath Introducers 2 06/24/2009 Arrow International Inc
Z-1502-2009 - Arrow OTW Percutaneous Thrombolytic Device (PTD) for fistulae and dialysis grafts 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-1490-2009 - Arrow Extension sets and accessories for intravascular use. 2 06/24/2009 Arrow International Inc
Z-1500-2009 - Arrow Balloon and stylet temporary pacing catheter 2 06/24/2009 Arrow International Inc
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