CATH. GUIDE 7F SR4.0 LAUNCHER CATHETER LA7SR40 LA 7F 100CM SR40 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 Code: LA7SR40
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-0976-06
- Quantity
- 362 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: 0000009532 0000013672 0000019809 0000022777 0000044800 0000045282 0000050729 0000056338 0000075247 0000076693 0000083944 0000096010 0000107906 0000123126 0000132923 175760 178292 180185 181735 182416 182417 183000 188007 203620 206606 212408 213693 219667
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.