TAG Medical Corp. Kibbutz Gaaton Naharia Israel Recalls

FDA
1
Total Recalls
1
Agencies
Feb 2016
First Recall
Feb 2016
Latest Recall

Showing 1-1 of 1 recalls

FDA

Tornier Arthro Tunneler. For transossous fixation of tendons to bone in rotator cuff repair. Catalog Number: SMB000101

Device failed to deploy the distal loop

Medicsense, the US Agent notified the sole distributor Tornier Inc., Edina, MN of the recall and requested notification to users requesting to discontinue and return product. Letter to customers dated December 4, 2009.