RecallDepth

6F Z2 GUIDING CATHETER SR5.0 CATHETER Z26SR50 Z2 6F 100CM SR50 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 Number: Z26SR50

This recall has been terminated (originally issued June 1, 2006).

Company
Medtronic, Inc.
Recall Initiated
April 5, 2006
Posted
June 1, 2006
Terminated
June 20, 2007
Recall Number
Z-1028-06
Quantity
81 units
Firm Location
Danvers, MA
Official Source
View on FDA website ↗

Reason for Recall

Potential for non-sterility due to loss of package integrity

Distribution

Nationwide 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.

Lot / Code Info

Lot Numbers: 0000060403 0000065850 0000140267 179669 209039 211282

Root Cause

Other

Action Taken

Medtronic 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.

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