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U.S. Department of Health and Human Services

Medical Device Recalls
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1 to 5 of 5 Results
510(K) Number: K990707
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FDA Recall
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Medtronic 6F Zuma Guide Catheter with AL 1.5 Curve with side holes Catalog Number: Z26AL15SH T... 2 06/26/2015 Medtronic Vascular
ZM5SR35 5F ZUMA SR3.5 CATHETER ZM5SR35 Z2 5F 100CM SR35 Coronary Guiding catheter designed to prov... 2 06/01/2006 Medtronic, Inc.
5F ZUMA SR5.0 Coronary Guiding catheter designed to provide a pathway through which therapeutic and... 2 06/01/2006 Medtronic, Inc.
5F ZUMA SR3.0 CATHETER ZM5SR30 Z2 5F 100CM SR30 Coronary Guiding catheter designed to provide a pa... 2 06/01/2006 Medtronic, Inc.
5F ZUMA SR4.0 CATHETER ZM5SR40 Z2 5F 100CM SR40 Coronary Guiding catheter designed to provide a pa... 2 06/01/2006 Medtronic, Inc.
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