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U.S. Department of Health and Human Services

Medical Device Recalls

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510(K) Number: K024050
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Product Description
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FDA Recall
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Ascend® AQ® Ureteral Dilation Balloon Catheter Set The Ascend® AQ® Ureteral Dilation Balloon Cathet... 2 03/24/2016 Cook Inc.
UltraxxTM Nephrostomy Balloon Set The Ultraxx" Nephrostomy Balloon Set consists of a radiopaque bal... 2 03/24/2016 Cook Inc.
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