ClearanceBrief
Recall Z-1061-06 ยท DQY Catheter, Percutaneous

Medtronic, Inc.

6F ZUMA DC3.5 W/110CM LENGTH GUID CATH 6F ZUMA DC 3.5 110CM Coronary Guiding catheter designed to provide a pathway through which therapeutic and/or diagnostic devices are introduced into the coronary or peripheral vascular system. Product Codes: ZM6DC35A , ZM6DC35A00

DateJun 1, 2006 (initiated Apr 5, 2006)
StatusTerminated
ReasonPotential for non-sterility due to loss of package integrity
Root causeOther
ActionMedtronic notified accounts and sales representatives on 4/05/06 advising the recalled product be segregated and held for return to the sales rep. and documented on the reconciliation form.
Quantity35 units
DistributionNationwide Foreign: Austria, Australia, Bahrain, Bulgaria, Canada, Czech Republic, Denmark, Germany, Hungary, Italy, Jordan, France, Greece, Japan, Hong Kong, India, Italy, Norway, Poland, Portugal, Saudi Arabia, Spain, Sweden, Switzerland, UK.
FDA recordOpen on fda.gov

510(k) clearances named in this recall

K981198MEDTRONIC ZUMA GUIDING CATHETER
Medtronics Interventional Vascular, Aug 7, 1998